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FDA 510(k)

Tyvek Roll with CI for STERLINK Sterilizer

K-Number: K223025 · 2023-05-09

Decision Date2023-05-09
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Tyvek Roll with CI for STERLINK Sterilizer is a medical device manufactured by Plasmapp Co,., Ltd.. It received FDA 510(k) clearance on 2023-05-09 under approval number K223025. 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 Tyvek Roll with CI for STERLINK Sterilizer?

Tyvek Roll with CI for STERLINK Sterilizer is a medical device that received FDA 510(k) clearance on 2023-05-09. It is manufactured by Plasmapp Co,., Ltd.. The 510(k) number is K223025.

When was Tyvek Roll with CI for STERLINK Sterilizer approved by the FDA?

Tyvek Roll with CI for STERLINK Sterilizer received FDA 510(k) clearance on 2023-05-09, under approval number K223025.

What company makes Tyvek Roll with CI for STERLINK Sterilizer?

Tyvek Roll with CI for STERLINK Sterilizer is manufactured by Plasmapp Co,., Ltd..

What is the FDA product code for Tyvek Roll with CI for STERLINK Sterilizer?

The FDA product code for Tyvek Roll with CI for STERLINK Sterilizer is FRG.

Other Devices by Plasmapp Co,., Ltd.

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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.