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FDA 510(k)

YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP

K-Number: K893409 · 1989-07-20

Decision Date1989-07-20
Product CodeBZT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP 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 1989-07-20 under 510(k) number K893409. The device is classified under product code BZT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP?

YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP is a medical device that received FDA 510(k) clearance on 1989-07-20. The listed applicant is Yellow Springs Instrument Co., Inc.. The 510(k) number is K893409.

When did YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP receive FDA 510(k) clearance?

YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP received FDA 510(k) clearance on 1989-07-20, under 510(k) number K893409.

Who is the listed applicant for YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP?

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 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP?

The FDA product code for YSI MODELS 4400 & 4700 ESOPHAGEAL STETHOSCOPE TEMP is BZT.

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: BZT)

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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