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FDA 510(k)

经测试可用于与化疗药物和低皮炎潜力一起使用的聚异戊二烯手术手套

K号: K230079 · 2023-08-23

决定日期2023-08-23
产品代码KGO
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决定实质等同

器械摘要

Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential is the device name listed in this FDA 510(k) record. The listed applicant is Ansell Healthcare Products, LLC. It received FDA 510(k) clearance on 2023-08-23 under 510(k) number K230079. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

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. The listed applicant is Ansell Healthcare Products, LLC. The 510(k) number is K230079.

When did Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential receive FDA 510(k) clearance?

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

Who is the listed applicant for Polyisoprene Surgical Gloves Tested for Use with Chemotherapy Drugs and Low Dermatitis Potential?

The FDA 510(k) record lists Ansell Healthcare Products, LLC as the applicant. This does not by itself establish the device manufacturer.

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.

相关临床试验

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列明Ansell Healthcare Products, LLC为申报人的其他记录

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相关器械(代码:KGO)

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官方来源

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