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FDA 510(k)

Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural)

K-Number: K221718 · 2022-09-24

Decision Date2022-09-24
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural) is a medical device manufactured by Hartalega NGC Sdn. Bhd.. It received FDA 510(k) clearance on 2022-09-24 under approval number K221718. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural)?

Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural) is a medical device that received FDA 510(k) clearance on 2022-09-24. It is manufactured by Hartalega NGC Sdn. Bhd.. The 510(k) number is K221718.

When was Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural) approved by the FDA?

Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural) received FDA 510(k) clearance on 2022-09-24, under approval number K221718.

What company makes Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural)?

Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural) is manufactured by Hartalega NGC Sdn. Bhd..

What is the FDA product code for Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural)?

The FDA product code for Polyisoprene Powder Free Surgical Glove Tested for Use with Chemotherapy Drugs (Natural) is KGO.

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Official Source

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