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FDA 510(k)

ELECTRONIC STETHOSCOPE #S-50

K-Number: K812148 · 1981-08-25

ApplicantSyphgmostat
Decision Date1981-08-25
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC STETHOSCOPE #S-50 is the device name listed in this FDA 510(k) record. The listed applicant is Syphgmostat. It received FDA 510(k) clearance on 1981-08-25 under 510(k) number K812148. 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 ELECTRONIC STETHOSCOPE #S-50?

ELECTRONIC STETHOSCOPE #S-50 is a medical device that received FDA 510(k) clearance on 1981-08-25. The listed applicant is Syphgmostat. The 510(k) number is K812148.

When did ELECTRONIC STETHOSCOPE #S-50 receive FDA 510(k) clearance?

ELECTRONIC STETHOSCOPE #S-50 received FDA 510(k) clearance on 1981-08-25, under 510(k) number K812148.

Who is the listed applicant for ELECTRONIC STETHOSCOPE #S-50?

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

What is the FDA product code for ELECTRONIC STETHOSCOPE #S-50?

The FDA product code for ELECTRONIC STETHOSCOPE #S-50 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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