FDA 510(k)

PVmed Contouring Software

Número K: K210916 · 2021-12-03

RequerentePerception Vision Medical Technologies Ltd.Co.

Data da decisão2021-12-03

Código do produtoLLZ

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

PVmed Contouring Software is the device name listed in this FDA 510(k) record. The listed applicant is Perception Vision Medical Technologies Ltd.Co.. It received FDA 510(k) clearance on 2021-12-03 under 510(k) number K210916. 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 PVmed Contouring Software?

PVmed Contouring Software is a medical device that received FDA 510(k) clearance on 2021-12-03. The listed applicant is Perception Vision Medical Technologies Ltd.Co.. The 510(k) number is K210916.

When did PVmed Contouring Software receive FDA 510(k) clearance?

PVmed Contouring Software received FDA 510(k) clearance on 2021-12-03, under 510(k) number K210916.

Who is the listed applicant for PVmed Contouring Software?

The FDA 510(k) record lists Perception Vision Medical Technologies Ltd.Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PVmed Contouring Software?

The FDA product code for PVmed Contouring Software is LLZ.

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