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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 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.

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. 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.

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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