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FDA 510(k)

ULTRA-VIOLET GLUCOSE REAGENT KIT

K-Number: K871456 · 1987-04-29

ApplicantBiochemical Trade, Inc.
Decision Date1987-04-29
Product CodeCFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ULTRA-VIOLET GLUCOSE REAGENT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Biochemical Trade, Inc.. It received FDA 510(k) clearance on 1987-04-29 under 510(k) number K871456. The device is classified under product code CFR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA-VIOLET GLUCOSE REAGENT KIT?

ULTRA-VIOLET GLUCOSE REAGENT KIT is a medical device that received FDA 510(k) clearance on 1987-04-29. The listed applicant is Biochemical Trade, Inc.. The 510(k) number is K871456.

When did ULTRA-VIOLET GLUCOSE REAGENT KIT receive FDA 510(k) clearance?

ULTRA-VIOLET GLUCOSE REAGENT KIT received FDA 510(k) clearance on 1987-04-29, under 510(k) number K871456.

Who is the listed applicant for ULTRA-VIOLET GLUCOSE REAGENT KIT?

The FDA 510(k) record lists Biochemical Trade, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRA-VIOLET GLUCOSE REAGENT KIT?

The FDA product code for ULTRA-VIOLET GLUCOSE REAGENT KIT is CFR.

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Related Devices (Code: CFR)

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.

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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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