YSI SERIES 500 THERMISTOR PROBES
K-Number: K792116 · 1980-01-16
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Device Summary
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.
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
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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