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FDA 510(k)

PLEXR PLUS

K-Number: K210693 · 2022-03-22

ApplicantGmv S.R.L.
Decision Date2022-03-22
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PLEXR PLUS is a medical device manufactured by Gmv S.R.L.. It received FDA 510(k) clearance on 2022-03-22 under approval number K210693. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLEXR PLUS?

PLEXR PLUS is a medical device that received FDA 510(k) clearance on 2022-03-22. It is manufactured by Gmv S.R.L.. The 510(k) number is K210693.

When was PLEXR PLUS approved by the FDA?

PLEXR PLUS received FDA 510(k) clearance on 2022-03-22, under approval number K210693.

What company makes PLEXR PLUS?

PLEXR PLUS is manufactured by Gmv S.R.L..

What is the FDA product code for PLEXR PLUS?

The FDA product code for PLEXR PLUS is GEI.

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Official Source

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