FDK

Primary DI
00859020006208
Brand
FDK
Company
FUDAKANG INDUSTRIAL LIMITED LIABILITY COMPANY
Model
FT-F33
Device description
FDK Non-Contact Infrared Thermometer
Published
2017-09-20
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
FLLThermometer, Electronic, Clinical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FLLContinuous Measurement ThermometerGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K111703000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K111703000INFRARED EAR THEROMETERFudakang Industrial Co., Ltd.2012-03-29FLL

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00859020006208PackageGS16In Commercial Distribution
00859020006215PackageGS196In Commercial Distribution
10859020006199PackageGS116In Commercial Distribution
00859020006192PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00859020006208008590200062088590200062080859020006208
00859020006215008590200062158590200062150859020006215
1085902000619910859020006199
00859020006192008590200061928590200061920859020006192

GMDN Terms#

Term, Definition table
TermDefinition
Infrared patient thermometer, skinA hand-held, battery-powered, electronic instrument designed to estimate the temperature of a site on the skin (e.g., axilla, forehead) by measurement of body infrared emissions at this particular point. It provides a method to determine temperature patterns or variations on the surface of the skin (e.g., due to differences in perfusion). This device may be used in the home. This is a reusable device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
030152184
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10859020006151FDKFT-E6882021-11-24
10859020006472FDKFT-F342020-08-11
10859020006434FDKBT-A132020-05-13
00859020006444FDKFT-F412020-03-31
20859020006066FDKFT-F312016-12-01
00859020006246FDKFT-C15Y2017-11-03
00859020006321FDKFT-C02-V (XL)2019-04-09

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Primary DI, Brand, Company table
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