UreTron PF Series Probe— 510(k) K162119
Substantially EquivalentMed-Sonics Corp.
FDA 510(k) clearance K162119 for UreTron PF Series Probe, Substantially Equivalent on 2016-08-29. Applicant: Med-Sonics Corp..
Clearance details
- Applicant
- Med-Sonics Corp.
- Product code
- Code FFK
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Erie, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.