FDA 510(k)

eClinic Stethopod

Numéro K : K220099 · 2022-10-20

Date de décision2022-10-20

Code produitDQD

Comité consultatifCV

DécisionSubstantially Equivalent

Résumé du dispositif

eClinic Stethopod is the device name listed in this FDA 510(k) record. The listed applicant is Homediagnostic, LLC. It received FDA 510(k) clearance on 2022-10-20 under 510(k) number K220099. 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 eClinic Stethopod?

eClinic Stethopod is a medical device that received FDA 510(k) clearance on 2022-10-20. The listed applicant is Homediagnostic, LLC. The 510(k) number is K220099.

When did eClinic Stethopod receive FDA 510(k) clearance?

eClinic Stethopod received FDA 510(k) clearance on 2022-10-20, under 510(k) number K220099.

Who is the listed applicant for eClinic Stethopod?

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

What is the FDA product code for eClinic Stethopod?

The FDA product code for eClinic Stethopod is DQD.

Essais cliniques associés

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Dispositifs connexes (Code : DQD)

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Source officielle

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