FDA 510(k)

GGM Breathing Circuit Bacterial Filter

Numéro K : K210352 · 2022-03-27

Date de décision2022-03-27

Code produitCAH

Comité consultatifAN

DécisionSubstantially Equivalent

Résumé du dispositif

GGM Breathing Circuit Bacterial Filter is the device name listed in this FDA 510(k) record. The listed applicant is Great Group Medical Co, Ltd.. It received FDA 510(k) clearance on 2022-03-27 under 510(k) number K210352. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the GGM Breathing Circuit Bacterial Filter?

GGM Breathing Circuit Bacterial Filter is a medical device that received FDA 510(k) clearance on 2022-03-27. The listed applicant is Great Group Medical Co, Ltd.. The 510(k) number is K210352.

When did GGM Breathing Circuit Bacterial Filter receive FDA 510(k) clearance?

GGM Breathing Circuit Bacterial Filter received FDA 510(k) clearance on 2022-03-27, under 510(k) number K210352.

Who is the listed applicant for GGM Breathing Circuit Bacterial Filter?

The FDA 510(k) record lists Great Group Medical Co, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GGM Breathing Circuit Bacterial Filter?

The FDA product code for GGM Breathing Circuit Bacterial Filter is CAH.

Essais cliniques associés

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Dispositifs connexes (Code : CAH)

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Source officielle

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