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FDA 510(k)

Sterilization Wrap

K-Number: K223600 · 2023-08-25

Decision Date2023-08-25
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sterilization Wrap is a medical device manufactured by Wuhan Zonsen Medical Products Co., Ltd.. It received FDA 510(k) clearance on 2023-08-25 under approval number K223600. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Sterilization Wrap?

Sterilization Wrap is a medical device that received FDA 510(k) clearance on 2023-08-25. It is manufactured by Wuhan Zonsen Medical Products Co., Ltd.. The 510(k) number is K223600.

When was Sterilization Wrap approved by the FDA?

Sterilization Wrap received FDA 510(k) clearance on 2023-08-25, under approval number K223600.

What company makes Sterilization Wrap?

Sterilization Wrap is manufactured by Wuhan Zonsen Medical Products Co., Ltd..

What is the FDA product code for Sterilization Wrap?

The FDA product code for Sterilization Wrap is FRG.

Other Devices by Wuhan Zonsen Medical Products Co., Ltd.

Related Devices (Code: FRG)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.