REPROCESSED ULTRASOUND INTRACARDIAC ECHO CATHETER— 510(k) K121913

Substantially Equivalent

Stryker Sustainability Solutions, Inc.

FDA 510(k) clearance K121913 for REPROCESSED ULTRASOUND INTRACARDIAC ECHO CATHETER, Substantially Equivalent on 2012-12-20. Applicant: Stryker Sustainability Solutions, Inc..

Clearance details

Applicant: Stryker Sustainability Solutions, Inc.
Product code: Code OWQ
Advisory panel: Cardiovascular
Date received: 2012-07-02
Decision date: 2012-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

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