FDA 510(k)

Patient Examination Gloves

Numéro K : K203593 · 2021-03-19

DemandeurGuangdong Kingfa Sci. & Tech.Co., Ltd.

Date de décision2021-03-19

Code produitLZA

Comité consultatifHO

DécisionSubstantially Equivalent

Résumé du dispositif

Patient Examination Gloves is the device name listed in this FDA 510(k) record. The listed applicant is Guangdong Kingfa Sci. & Tech.Co., Ltd.. It received FDA 510(k) clearance on 2021-03-19 under 510(k) number K203593. 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 Patient Examination Gloves?

Patient Examination Gloves is a medical device that received FDA 510(k) clearance on 2021-03-19. The listed applicant is Guangdong Kingfa Sci. & Tech.Co., Ltd.. The 510(k) number is K203593.

When did Patient Examination Gloves receive FDA 510(k) clearance?

Patient Examination Gloves received FDA 510(k) clearance on 2021-03-19, under 510(k) number K203593.

Who is the listed applicant for Patient Examination Gloves?

The FDA 510(k) record lists Guangdong Kingfa Sci. & Tech.Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Patient Examination Gloves?

The FDA product code for Patient Examination Gloves is LZA.

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Autres dossiers indiquant Guangdong Kingfa Sci. & Tech.Co., Ltd. en tant que demandeur

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Dispositifs connexes (Code : LZA)

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Source officielle

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