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FDA 510(k)

Viveve System

K-Number: K200472 · 2020-11-18

ApplicantViveve Medical, Inc.
Decision Date2020-11-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Viveve System is a medical device manufactured by Viveve Medical, Inc.. It received FDA 510(k) clearance on 2020-11-18 under approval number K200472. 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 Viveve System?

Viveve System is a medical device that received FDA 510(k) clearance on 2020-11-18. It is manufactured by Viveve Medical, Inc.. The 510(k) number is K200472.

When was Viveve System approved by the FDA?

Viveve System received FDA 510(k) clearance on 2020-11-18, under approval number K200472.

What company makes Viveve System?

Viveve System is manufactured by Viveve Medical, Inc..

What is the FDA product code for Viveve System?

The FDA product code for Viveve System is GEI.

Other Devices by Viveve Medical, Inc.

K193611Viveve 2.0 System K212678Viveve System, Viveve 2.0 System

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Official Source

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