FDA 510(k)

ELECTRONIC STETHOSCOPE

K-Number: K761308 · 1977-01-06

Decision Date1977-01-06

Product CodeDPD

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

ELECTRONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1977-01-06 under 510(k) number K761308. The device is classified under product code DPD. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRONIC STETHOSCOPE?

ELECTRONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 1977-01-06. The listed applicant is Medline Industries, Inc.. The 510(k) number is K761308.

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

ELECTRONIC STETHOSCOPE received FDA 510(k) clearance on 1977-01-06, under 510(k) number K761308.

Who is the listed applicant for ELECTRONIC STETHOSCOPE?

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

What is the FDA product code for ELECTRONIC STETHOSCOPE?

The FDA product code for ELECTRONIC STETHOSCOPE is DPD.

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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.