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FDA 510(k)

GLUCOSE (HEXOKINASE)

K-Number: K874846 · 1988-03-03

ApplicantTech-Co, Inc.
Decision Date1988-03-03
Product CodeCFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOSE (HEXOKINASE) is the device name listed in this FDA 510(k) record. The listed applicant is Tech-Co, Inc.. It received FDA 510(k) clearance on 1988-03-03 under 510(k) number K874846. 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)?

GLUCOSE (HEXOKINASE) is a medical device that received FDA 510(k) clearance on 1988-03-03. The listed applicant is Tech-Co, Inc.. The 510(k) number is K874846.

When did GLUCOSE (HEXOKINASE) receive FDA 510(k) clearance?

GLUCOSE (HEXOKINASE) received FDA 510(k) clearance on 1988-03-03, under 510(k) number K874846.

Who is the listed applicant for GLUCOSE (HEXOKINASE)?

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

What is the FDA product code for GLUCOSE (HEXOKINASE)?

The FDA product code for GLUCOSE (HEXOKINASE) is CFR.

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Other records listing Tech-Co, Inc. as applicant

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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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