FDA 510(k)

Feelix Stethoscope

Numéro K : K200862 · 2020-09-14

Date de décision2020-09-14

Code produitDQD

Comité consultatifCV

DécisionSubstantially Equivalent

Résumé du dispositif

Feelix Stethoscope is the device name listed in this FDA 510(k) record. The listed applicant is Sonavi Labs, Inc.. It received FDA 510(k) clearance on 2020-09-14 under 510(k) number K200862. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Feelix Stethoscope?

Feelix Stethoscope is a medical device that received FDA 510(k) clearance on 2020-09-14. The listed applicant is Sonavi Labs, Inc.. The 510(k) number is K200862.

When did Feelix Stethoscope receive FDA 510(k) clearance?

Feelix Stethoscope received FDA 510(k) clearance on 2020-09-14, under 510(k) number K200862.

Who is the listed applicant for Feelix Stethoscope?

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

What is the FDA product code for Feelix Stethoscope?

The FDA product code for Feelix Stethoscope is DQD.

Essais cliniques associés

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Dispositifs connexes (Code : DQD)

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Source officielle

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