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FDA 510(k)

YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE

K-Number: K962070 · 1996-07-19

Decision Date1996-07-19
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE 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 1996-07-19 under 510(k) number K962070. 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 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE?

YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE is a medical device that received FDA 510(k) clearance on 1996-07-19. The listed applicant is Yellow Springs Instrument Co., Inc.. The 510(k) number is K962070.

When did YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE receive FDA 510(k) clearance?

YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE received FDA 510(k) clearance on 1996-07-19, under 510(k) number K962070.

Who is the listed applicant for YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE?

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 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE?

The FDA product code for YSI 400 SERIES ATUOCLAVABLE REUSABLE TEMPERATURE PROBE 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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