FDA.reportPublic FDA data

HealthyMe Early Detection Pregnancy Test

Primary DI
00682607630554
Brand
HealthyMe Early Detection Pregnancy Test
Company
Acon Laboratories, Inc.
Model
L031-20198-103
Catalog number
763055
Device description
Early Detection Pregnancy Test
Published
2024-03-27
Public version status
Update
Distribution status
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
K193318000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K193318000Distinct® Early Detection Pregnancy TestACON Laboratories, Inc.2020-08-20LCX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10682607630551PackageGS16In Commercial Distribution
20682607630558PackageGS16In Commercial Distribution
00682607630554PrimaryGS10
00682607003242Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1068260763055110682607630551
2068260763055820682607630558
00682607630554006826076305546826076305540682607630554
00682607003242006826070032426826070032420682607003242

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 Temperature36 Degrees Fahrenheit86 Degrees Fahrenheit

Contacts#

Phone, Email table
PhoneEmail
+1(800)838-9502support@aconlabs.com

Regulatory Flags#

DUNS number
781100966
Device count
3
Lot or batch
true
Expiration date on label
true

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10682607690074Mission Cholesterol Optical Check DeviceC121-2021C121-20212026-03-09
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20682607200485Mission U120 Smart Urine AnalyzerU117-1012026-02-06
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