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FDA 510(k)

GLUCOSE HEXOKINASE

K-Number: K880236 · 1988-03-15

ApplicantTech-Neal Scientific, Inc.
Decision Date1988-03-15
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-Neal Scientific, Inc.. It received FDA 510(k) clearance on 1988-03-15 under 510(k) number K880236. 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 1988-03-15. The listed applicant is Tech-Neal Scientific, Inc.. The 510(k) number is K880236.

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

GLUCOSE HEXOKINASE received FDA 510(k) clearance on 1988-03-15, under 510(k) number K880236.

Who is the listed applicant for GLUCOSE HEXOKINASE?

The FDA 510(k) record lists Tech-Neal Scientific, 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-Neal Scientific, 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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