RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER— 510(k) K073041

Substantially Equivalent

Acclarent, Inc.

FDA 510(k) clearance K073041 for RELIEVA AND RELIEVA ACELLA SINUS BALLOON CATHETER, Substantially Equivalent on 2008-03-11. Applicant: Acclarent, Inc..

Clearance details

Applicant: Acclarent, Inc.
Product code: Code KAM
Advisory panel: General, Plastic Surgery
Date received: 2007-10-29
Decision date: 2008-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rmenlo Park, CA, US

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