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FDA 510(k)

Ambient HipVac 50 Wand with Integrated Finger Switches

K-Number: K161481 · 2016-10-21

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

Device Summary

Ambient HipVac 50 Wand with Integrated Finger Switches is the device name listed in this FDA 510(k) record. The listed applicant is ArthroCare Corporation. It received FDA 510(k) clearance on 2016-10-21 under 510(k) 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. The listed applicant is ArthroCare Corporation. The 510(k) number is K161481.

When did Ambient HipVac 50 Wand with Integrated Finger Switches receive FDA 510(k) clearance?

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

Who is the listed applicant for Ambient HipVac 50 Wand with Integrated Finger Switches?

The FDA 510(k) record lists ArthroCare Corporation as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing ArthroCare Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: GEI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261179AlphaTriPart - Monopolar MIC InstrumentsGimmi GmbHK253504Volnewmer™Classys, Inc.K254056THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type S (TB-0545FCS); THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S (TB-0535FCS); THUNDERBEAT 5 mm, 20 cm, Front-actuated Grip Type S (TB-0520FCS)Olympus Medical Systems Corp.K253484LUTRONIC GENIUSCynosure Lutronic Technology CorporationK251492Irrigation Tubing Bipolar Cord SetNew Deantronics Taiwan , Ltd.K260636Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coatingStryker Sustainability Solutions

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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