VPULSE— 510(k) K122640

Substantially Equivalent

Cothera, LLC

FDA 510(k) clearance K122640 for VPULSE, Substantially Equivalent on 2013-02-22. Applicant: Cothera, LLC.

Clearance details

Applicant: Cothera, LLC
Product code: Code JOW
Advisory panel: Cardiovascular
Date received: 2012-08-29
Decision date: 2013-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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