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FDA 510(k)

PVmed Contouring Software

K-Number: K210916 · 2021-12-03

ApplicantPerception Vision Medical Technologies Ltd.Co.
Decision Date2021-12-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PVmed Contouring Software is a medical device manufactured by Perception Vision Medical Technologies Ltd.Co.. It received FDA 510(k) clearance on 2021-12-03 under approval number K210916. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PVmed Contouring Software?

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

When was PVmed Contouring Software approved by the FDA?

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

What company makes PVmed Contouring Software?

PVmed Contouring Software is manufactured by Perception Vision Medical Technologies Ltd.Co..

What is the FDA product code for PVmed Contouring Software?

The FDA product code for PVmed Contouring Software is LLZ.

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Official Source

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