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FDA 510(k)

AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches

K-Number: K180848 · 2018-05-01

ApplicantArthroCare Corporation
Decision Date2018-05-01
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches is a medical device manufactured by ArthroCare Corporation. It received FDA 510(k) clearance on 2018-05-01 under approval number K180848. 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 Super MULTIVAC 50 Wand with Integrated Finger Switches?

AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches is a medical device that received FDA 510(k) clearance on 2018-05-01. It is manufactured by ArthroCare Corporation. The 510(k) number is K180848.

When was AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches approved by the FDA?

AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches received FDA 510(k) clearance on 2018-05-01, under approval number K180848.

What company makes AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches?

AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches is manufactured by ArthroCare Corporation.

What is the FDA product code for AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches?

The FDA product code for AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches is GEI.

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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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