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FDA 510(k)

GLUCOSE OXIDASE

K-Number: K863926 · 1986-11-13

ApplicantTech-Co, Inc.
Decision Date1986-11-13
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GLUCOSE OXIDASE 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 1986-11-13 under 510(k) number K863926. The device is classified under product code CGA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLUCOSE OXIDASE?

GLUCOSE OXIDASE is a medical device that received FDA 510(k) clearance on 1986-11-13. The listed applicant is Tech-Co, Inc.. The 510(k) number is K863926.

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

GLUCOSE OXIDASE received FDA 510(k) clearance on 1986-11-13, under 510(k) number K863926.

Who is the listed applicant for GLUCOSE OXIDASE?

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 OXIDASE?

The FDA product code for GLUCOSE OXIDASE is CGA.

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Other records listing Tech-Co, Inc. as applicant

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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Related Devices (Code: CGA)

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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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