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FDA 510(k)

Ambient HipVac 50 Wand with Integrated Finger Switches

K-Number: K161481 · 2016-10-21

Decision Date2016-10-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Ambient HipVac 50 Wand with Integrated Finger Switches is a medical device manufactured by ArthroCare Corporation. It received FDA 510(k) clearance on 2016-10-21 under approval number K161481. 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 Ambient HipVac 50 Wand with Integrated Finger Switches?

Ambient HipVac 50 Wand with Integrated Finger Switches is a medical device that received FDA 510(k) clearance on 2016-10-21. It is manufactured by ArthroCare Corporation. The 510(k) number is K161481.

When was Ambient HipVac 50 Wand with Integrated Finger Switches approved by the FDA?

Ambient HipVac 50 Wand with Integrated Finger Switches received FDA 510(k) clearance on 2016-10-21, under approval number K161481.

What company makes Ambient HipVac 50 Wand with Integrated Finger Switches?

Ambient HipVac 50 Wand with Integrated Finger Switches is manufactured by ArthroCare Corporation.

What is the FDA product code for Ambient HipVac 50 Wand with Integrated Finger Switches?

The FDA product code for Ambient HipVac 50 Wand with Integrated Finger Switches is GEI.

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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.