FDA 510(k)

PP Care Nitrile Examination Gloves

Numéro K : K212629 · 2022-05-26

DemandeurEg Group Product and Services Co., Ltd.

Date de décision2022-05-26

Code produitLZA

Comité consultatifHO

DécisionSubstantially Equivalent

Résumé du dispositif

PP Care Nitrile Examination Gloves is the device name listed in this FDA 510(k) record. The listed applicant is Eg Group Product and Services Co., Ltd.. It received FDA 510(k) clearance on 2022-05-26 under 510(k) number K212629. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the PP Care Nitrile Examination Gloves?

PP Care Nitrile Examination Gloves is a medical device that received FDA 510(k) clearance on 2022-05-26. The listed applicant is Eg Group Product and Services Co., Ltd.. The 510(k) number is K212629.

When did PP Care Nitrile Examination Gloves receive FDA 510(k) clearance?

PP Care Nitrile Examination Gloves received FDA 510(k) clearance on 2022-05-26, under 510(k) number K212629.

Who is the listed applicant for PP Care Nitrile Examination Gloves?

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

What is the FDA product code for PP Care Nitrile Examination Gloves?

The FDA product code for PP Care Nitrile Examination Gloves is LZA.

Essais cliniques associés

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Dispositifs connexes (Code : LZA)

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Source officielle

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