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FDA 510(k)

GO/HPO-GLUCOSE REAGENT (TRINDER)

K-Number: K770200 · 1977-02-23

ApplicantBeckman Instruments, Inc.
Decision Date1977-02-23
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GO/HPO-GLUCOSE REAGENT (TRINDER) is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1977-02-23 under 510(k) number K770200. 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 GO/HPO-GLUCOSE REAGENT (TRINDER)?

GO/HPO-GLUCOSE REAGENT (TRINDER) is a medical device that received FDA 510(k) clearance on 1977-02-23. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K770200.

When did GO/HPO-GLUCOSE REAGENT (TRINDER) receive FDA 510(k) clearance?

GO/HPO-GLUCOSE REAGENT (TRINDER) received FDA 510(k) clearance on 1977-02-23, under 510(k) number K770200.

Who is the listed applicant for GO/HPO-GLUCOSE REAGENT (TRINDER)?

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

What is the FDA product code for GO/HPO-GLUCOSE REAGENT (TRINDER)?

The FDA product code for GO/HPO-GLUCOSE REAGENT (TRINDER) is CGA.

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Other records listing Beckman Instruments, Inc. as applicant

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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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