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FDA 510(k)

leva Pelvic Health System

K-Number: K213913 · 2022-06-30

ApplicantRenovia, Inc.
Decision Date2022-06-30
Product CodeHIR
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

leva Pelvic Health System is a medical device manufactured by Renovia, Inc.. It received FDA 510(k) clearance on 2022-06-30 under approval number K213913. The device is classified under product code HIR. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the leva Pelvic Health System?

leva Pelvic Health System is a medical device that received FDA 510(k) clearance on 2022-06-30. It is manufactured by Renovia, Inc.. The 510(k) number is K213913.

When was leva Pelvic Health System approved by the FDA?

leva Pelvic Health System received FDA 510(k) clearance on 2022-06-30, under approval number K213913.

What company makes leva Pelvic Health System?

leva Pelvic Health System is manufactured by Renovia, Inc..

What is the FDA product code for leva Pelvic Health System?

The FDA product code for leva Pelvic Health System is HIR.

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Official Source

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