FDA 510(k)

Steiking Packaging for Medical Devices

Número K: K210810 · 2022-01-23

Data da decisão2022-01-23

Código do produtoFRG

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Steiking 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 2022-01-23 under 510(k) number K210810. 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 Steiking Packaging for Medical Devices?

Steiking Packaging for Medical Devices is a medical device that received FDA 510(k) clearance on 2022-01-23. The listed applicant is Wipak OY. The 510(k) number is K210810.

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

Steiking Packaging for Medical Devices received FDA 510(k) clearance on 2022-01-23, under 510(k) number K210810.

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

The FDA product code for Steiking 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 K221016Steriking Packaging for Medical Devices

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Fonte oficial

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