FDA 510(k)

Steriking Packaging for Medical Devices

Número K: K221016 · 2022-05-05

Data da decisão2022-05-05

Código do produtoFRG

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Steriking Packaging for Medical Devices is the device name listed in this FDA 510(k) record. The listed applicant is Wipak OY. It received FDA 510(k) clearance on 2022-05-05 under 510(k) number K221016. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Steriking Packaging for Medical Devices?

Steriking Packaging for Medical Devices is a medical device that received FDA 510(k) clearance on 2022-05-05. The listed applicant is Wipak OY. The 510(k) number is K221016.

When did Steriking Packaging for Medical Devices receive FDA 510(k) clearance?

Steriking Packaging for Medical Devices received FDA 510(k) clearance on 2022-05-05, under 510(k) number K221016.

Who is the listed applicant for Steriking Packaging for Medical Devices?

The FDA 510(k) record lists Wipak OY as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Steriking Packaging for Medical Devices?

The FDA product code for Steriking Packaging for Medical Devices is FRG.

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Outros registros que listam Wipak OY como candidato(a)

K232625Steriking® Pouch for Robotic Instruments K231999Steriking® LT-Blueline Pouches with Tyvek®K231996Steriking® LT-Blueline Pouches with Tyvek®K221379Steriking LT-Blueline Pouches with Tyvek K221377SteriKing LT-Blueline Pouches with Tyvek K210810Steiking Packaging for Medical Devices

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Fonte oficial

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