REPROCESSED ULTRASOUND INTRACARDIAC ECHO CATHETER— 510(k) K121913
Substantially EquivalentStryker 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.. Device class: 2.
Clearance details
- Applicant
- Stryker Sustainability Solutions, Inc.
- Product code
- Code OWQ
- Device class
- Class 2
- Regulation
- 21 CFR 870.1200
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Phoenix, AZ, US
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More clearances from Stryker Sustainability Solutions, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.