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FDA 510(k)

YSI SERIES 500 THERMISTOR PROBES

K-Number: K792116 · 1980-01-16

Decision Date1980-01-16
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

YSI SERIES 500 THERMISTOR PROBES 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 1980-01-16 under 510(k) number K792116. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YSI SERIES 500 THERMISTOR PROBES?

YSI SERIES 500 THERMISTOR PROBES is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is Yellow Springs Instrument Co., Inc.. The 510(k) number is K792116.

When did YSI SERIES 500 THERMISTOR PROBES receive FDA 510(k) clearance?

YSI SERIES 500 THERMISTOR PROBES received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792116.

Who is the listed applicant for YSI SERIES 500 THERMISTOR PROBES?

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 SERIES 500 THERMISTOR PROBES?

The FDA product code for YSI SERIES 500 THERMISTOR PROBES is FLL.

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: FLL)

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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