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FDA 510(k)

YSI #24 & 24M GLUCOSE ANALYZERS

K-Number: K821192 · 1982-06-14

Decision Date1982-06-14
Product CodeCGA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

YSI #24 & 24M GLUCOSE ANALYZERS is the device name listed in this FDA 510(k) record. The listed applicant is Yellow Springs Instrument Co., Inc.. It received FDA 510(k) clearance on 1982-06-14 under 510(k) number K821192. 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 YSI #24 & 24M GLUCOSE ANALYZERS?

YSI #24 & 24M GLUCOSE ANALYZERS is a medical device that received FDA 510(k) clearance on 1982-06-14. The listed applicant is Yellow Springs Instrument Co., Inc.. The 510(k) number is K821192.

When did YSI #24 & 24M GLUCOSE ANALYZERS receive FDA 510(k) clearance?

YSI #24 & 24M GLUCOSE ANALYZERS received FDA 510(k) clearance on 1982-06-14, under 510(k) number K821192.

Who is the listed applicant for YSI #24 & 24M GLUCOSE ANALYZERS?

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

What is the FDA product code for YSI #24 & 24M GLUCOSE ANALYZERS?

The FDA product code for YSI #24 & 24M GLUCOSE ANALYZERS is CGA.

Related Clinical Trials

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.

Other records listing Yellow Springs Instrument 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.

View all 23 devices →

Related Devices (Code: CGA)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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