FDA 510(k)

YSI MODELS 23C & 23CM HDL & TOTAL CHOLES

K-Number: K801285 · 1980-07-28

ApplicantYellow Springs Instrument Co., Inc.

Decision Date1980-07-28

Product CodeCHH

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

YSI MODELS 23C & 23CM HDL & TOTAL CHOLES 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 1980-07-28 under 510(k) number K801285. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YSI MODELS 23C & 23CM HDL & TOTAL CHOLES?

YSI MODELS 23C & 23CM HDL & TOTAL CHOLES is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Yellow Springs Instrument Co., Inc.. The 510(k) number is K801285.

When did YSI MODELS 23C & 23CM HDL & TOTAL CHOLES receive FDA 510(k) clearance?

YSI MODELS 23C & 23CM HDL & TOTAL CHOLES received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801285.

Who is the listed applicant for YSI MODELS 23C & 23CM HDL & TOTAL CHOLES?

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 MODELS 23C & 23CM HDL & TOTAL CHOLES?

The FDA product code for YSI MODELS 23C & 23CM HDL & TOTAL CHOLES is CHH.

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Related Devices (Code: CHH)

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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.