FDA.reportPublic FDA data

Health Mart

Primary DI
00052569143810
Brand
Health Mart
Company
MCKESSON CORPORATION
Model
One Step Pregnancy Test
Device description
Health Mart DPS +/- Blue Cap
Published
2020-09-28
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LCXKit, Test, Pregnancy, Hcg, Over The Counter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LCXKit, Test, Pregnancy, Hcg, Over The CounterClinical Chemistry2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K042280000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K042280000FACT PLUS ONE-STEP PREGNANCY TEST KITUnipath , Ltd.2004-09-10LCX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10052569143817PackageGS124Not in Commercial Distribution
00052569143810PrimaryGS10
00633472000133Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1005256914381710052569143817
00052569143810000525691438100525691438100052569143810
00633472000133006334720001336334720001330633472000133

GMDN Terms#

Term, Definition table
TermDefinition
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinicalA collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of total human chorionic gonadotropin (HCG), which includes a combination of intact HCG, nicked HCG, alpha-HCG subunits, and beta-HCG subunits, in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses to aid detection of pregnancy, or as a predictor of adverse pregnancy outcomes (e.g., miscarriage) and/or trisomy 21 (Down syndrome). It is not intended to be used for self-testing.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Temperature2 Degrees Celsius30 Degrees Celsius

Contacts#

Phone, Email table
PhoneEmail
1-800-899-7353xx@xx.xx

Regulatory Flags#

DUNS number
177667227
Device count
2
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00010939960139Foster & ThriveBP3NP1-3EMFT(2878056)2024-09-23
00010939960153Foster & ThriveBP3NU1-3EMFT(2878072)2024-09-23
00010939960177Foster & ThriveBP3MV1-3BMFT(2878098)2024-09-23
10010939960136Foster & ThriveBP3NP1-3EMFT(2878056)2024-09-23
10010939960150Foster & ThriveBP3NU1-3EMFT(2878072)2024-09-23
10010939960174Foster & ThriveBP3MV1-3BMFT(2878098)2024-09-23
00010939960191Foster & ThriveKD-1541.F&T2024-07-23
00010939960207Foster & ThriveK-955.F&T2024-07-23
00010939960214Foster & ThriveKD-2280.F&T2024-07-23
00010939960221Foster & ThriveKD-1540.F&T2024-07-23
00010939960238Foster & ThriveKD-1780-1.F&T2024-07-23
20010939960195Foster & ThriveKD-1541.F&T2024-07-23
20010939960201Foster & ThriveK-955.F&T2024-07-23
20010939960218Foster & ThriveKD-2280.F&T2024-07-23
20010939960225Foster & ThriveKD-1540.F&T2024-07-23
20010939960232Foster & ThriveKD-1780-1.F&T2024-07-23
00010939960160Foster & ThriveBP3NM1-3WMFT(2878080)2024-06-21
10010939960167Foster & ThriveBP3NM1-3WMFT(2878080)2024-06-21
00010939960146Foster & ThriveBP3NG1-1AMFT(2878064)2024-06-19
00010939960184Foster & ThriveBPAG1-20MFT(2878106)2024-06-18

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Primary DI, Brand, Company table
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06950996006323Orient GeneZhejiang Orient Gene Biotech Co.,Ltd.LCX2026-07-23
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06950996067577Orient GeneZhejiang Orient Gene Biotech Co.,Ltd.LCX2026-07-23
06923304600124FERTICAREWeihai Kangzhou Biotechnology Engineering Co., LtdLCX2026-07-21
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