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FDA 510(k)

Patient Examination Gloves

K-Number: K203593 · 2021-03-19

Decision Date2021-03-19
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Patient Examination Gloves is a medical device manufactured by Guangdong Kingfa Sci. & Tech.Co., Ltd.. It received FDA 510(k) clearance on 2021-03-19 under approval number K203593. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Patient Examination Gloves?

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

When was Patient Examination Gloves approved by the FDA?

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

What company makes Patient Examination Gloves?

Patient Examination Gloves is manufactured by Guangdong Kingfa Sci. & Tech.Co., Ltd..

What is the FDA product code for Patient Examination Gloves?

The FDA product code for Patient Examination Gloves is LZA.

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Official Source

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