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FDA 510(k)

STETHOSCOPE, ELECTRONIC

K-Number: K772173 · 1978-01-24

ApplicantAffiliated Mailorder Co. Sales, Inc.
Decision Date1978-01-24
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STETHOSCOPE, ELECTRONIC is the device name listed in this FDA 510(k) record. The listed applicant is Affiliated Mailorder Co. Sales, Inc.. It received FDA 510(k) clearance on 1978-01-24 under 510(k) number K772173. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STETHOSCOPE, ELECTRONIC?

STETHOSCOPE, ELECTRONIC is a medical device that received FDA 510(k) clearance on 1978-01-24. The listed applicant is Affiliated Mailorder Co. Sales, Inc.. The 510(k) number is K772173.

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

STETHOSCOPE, ELECTRONIC received FDA 510(k) clearance on 1978-01-24, under 510(k) number K772173.

Who is the listed applicant for STETHOSCOPE, ELECTRONIC?

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

What is the FDA product code for STETHOSCOPE, ELECTRONIC?

The FDA product code for STETHOSCOPE, ELECTRONIC is DQD.

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Related Devices (Code: DQD)

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.

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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.

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