WavelinQ Generator
K-Number: K222793 · 2022-10-17
ApplicantC.R. Bard, Inc.
Decision Date2022-10-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
WavelinQ Generator is a medical device manufactured by C.R. Bard, Inc.. It received FDA 510(k) clearance on 2022-10-17 under approval number K222793. 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 WavelinQ Generator?
WavelinQ Generator is a medical device that received FDA 510(k) clearance on 2022-10-17. It is manufactured by C.R. Bard, Inc.. The 510(k) number is K222793.
When was WavelinQ Generator approved by the FDA?
WavelinQ Generator received FDA 510(k) clearance on 2022-10-17, under approval number K222793.
What company makes WavelinQ Generator?
WavelinQ Generator is manufactured by C.R. Bard, Inc..
What is the FDA product code for WavelinQ Generator?
The FDA product code for WavelinQ Generator is GEI.
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Official Source
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