FDA 510(k)

ImmersiveTouch

Número K: K210726 · 2021-09-29

Data da decisão2021-09-29

Código do produtoLLZ

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

ImmersiveTouch is the device name listed in this FDA 510(k) record. The listed applicant is Immersivetouch, Inc.. It received FDA 510(k) clearance on 2021-09-29 under 510(k) number K210726. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the ImmersiveTouch?

ImmersiveTouch is a medical device that received FDA 510(k) clearance on 2021-09-29. The listed applicant is Immersivetouch, Inc.. The 510(k) number is K210726.

When did ImmersiveTouch receive FDA 510(k) clearance?

ImmersiveTouch received FDA 510(k) clearance on 2021-09-29, under 510(k) number K210726.

Who is the listed applicant for ImmersiveTouch?

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

What is the FDA product code for ImmersiveTouch?

The FDA product code for ImmersiveTouch is LLZ.

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