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FDA 510(k)

DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS

K-Number: K931474 · 1994-05-10

ApplicantGbf Medical Group
Decision Date1994-05-10
Product CodeKDW
Advisory CommitteePA
DecisionUnknown

Device Summary

DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS is the device name listed in this FDA 510(k) record. The listed applicant is Gbf Medical Group. It received FDA 510(k) clearance on 1994-05-10 under 510(k) number K931474. The device is classified under product code KDW. It was reviewed by the PA advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS?

DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS is a medical device that received FDA 510(k) clearance on 1994-05-10. The listed applicant is Gbf Medical Group. The 510(k) number is K931474.

When did DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS receive FDA 510(k) clearance?

DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS received FDA 510(k) clearance on 1994-05-10, under 510(k) number K931474.

Who is the listed applicant for DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS?

The FDA 510(k) record lists Gbf Medical Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS?

The FDA product code for DRUG, INSURANCE, URINALYSIS, BLOOD/URINE TEST KITS is KDW.

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Related Devices (Code: KDW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K970580SASI-DC1TSSubstance Abuse Specialties, Inc.K951122CAPITOL URINE DRUG SCREEN COLLECTION KITHarry A. SchlakmanK913967DOX TAMPERPROOF SPECIMEN CONTAINER SYSTEMDoxtech, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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