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FDA 510(k)

OLYMPUS GLUCOSE REAGENT

K-Number: K924601 · 1992-12-03

ApplicantOlympus Corp.
Decision Date1992-12-03
Product CodeCFR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

OLYMPUS GLUCOSE REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1992-12-03 under 510(k) number K924601. 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 OLYMPUS GLUCOSE REAGENT?

OLYMPUS GLUCOSE REAGENT is a medical device that received FDA 510(k) clearance on 1992-12-03. The listed applicant is Olympus Corp.. The 510(k) number is K924601.

When did OLYMPUS GLUCOSE REAGENT receive FDA 510(k) clearance?

OLYMPUS GLUCOSE REAGENT received FDA 510(k) clearance on 1992-12-03, under 510(k) number K924601.

Who is the listed applicant for OLYMPUS GLUCOSE REAGENT?

The FDA 510(k) record lists Olympus Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPUS GLUCOSE REAGENT?

The FDA product code for OLYMPUS GLUCOSE REAGENT is CFR.

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Other records listing Olympus Corp. as applicant

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K915402EW-10 AND EW-20K933200OLYMPUS PBD STENTSK942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIESK931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESSK934835FLOVALK931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

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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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