FDA 510(k)

AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches

K-번호: K180848 · 2018-05-01

결정일2018-05-01

제품 코드GEI

자문 위원회SU

결정Substantially Equivalent

기기 요약

AMBIENT Super MULTIVAC 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 2018-05-01 under 510(k) number K180848. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

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. The listed applicant is ArthroCare Corporation. The 510(k) number is K180848.

When did AMBIENT Super MULTIVAC 50 Wand with Integrated Finger Switches receive FDA 510(k) clearance?

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

Who is the listed applicant for AMBIENT Super MULTIVAC 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 Super MULTIVAC 50 Wand with Integrated Finger Switches?

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

ArthroCare Corporation를 신청인으로 등재한 기타 기록

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