FDA 510(k)

GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600

K-Number: K896028 · 1989-11-14

Decision Date1989-11-14

Product CodeCFR

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600 is the device name listed in this FDA 510(k) record. The listed applicant is American Research Products Co.. It received FDA 510(k) clearance on 1989-11-14 under 510(k) number K896028. 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 GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600?

GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600 is a medical device that received FDA 510(k) clearance on 1989-11-14. The listed applicant is American Research Products Co.. The 510(k) number is K896028.

When did GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600 receive FDA 510(k) clearance?

GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600 received FDA 510(k) clearance on 1989-11-14, under 510(k) number K896028.

Who is the listed applicant for GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600?

The FDA 510(k) record lists American Research Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600?

The FDA product code for GLUCOSE-HEXOKINASE REAGENTS 4470030,050,300,600 is CFR.

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Official Source

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