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FDA 510(k)

Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential

K-Number: K230079 · 2023-08-23

Decision Date2023-08-23
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential is a medical device manufactured by Ansell Healthcare Products, LLC. It received FDA 510(k) clearance on 2023-08-23 under approval number K230079. 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 Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential?

Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential is a medical device that received FDA 510(k) clearance on 2023-08-23. It is manufactured by Ansell Healthcare Products, LLC. The 510(k) number is K230079.

When was Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential approved by the FDA?

Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential received FDA 510(k) clearance on 2023-08-23, under approval number K230079.

What company makes Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential?

Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential is manufactured by Ansell Healthcare Products, LLC.

What is the FDA product code for Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential?

The FDA product code for Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential is KGO.

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Official Source

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