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FDA 510(k)

ULTRASONIC STETHOSCOPE

K-Number: K803246 · 1981-01-28

ApplicantSonicaid, Inc.
Decision Date1981-01-28
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRASONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Sonicaid, Inc.. It received FDA 510(k) clearance on 1981-01-28 under 510(k) number K803246. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASONIC STETHOSCOPE?

ULTRASONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1981-01-28. The listed applicant is Sonicaid, Inc.. The 510(k) number is K803246.

When did ULTRASONIC STETHOSCOPE receive FDA 510(k) clearance?

ULTRASONIC STETHOSCOPE received FDA 510(k) clearance on 1981-01-28, under 510(k) number K803246.

Who is the listed applicant for ULTRASONIC STETHOSCOPE?

The FDA 510(k) record lists Sonicaid, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRASONIC STETHOSCOPE?

The FDA product code for ULTRASONIC STETHOSCOPE is IYN.

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Related Devices (Code: IYN)

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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.

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