Avulsion Forceps— 510(k) K183428
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K183428 for Avulsion Forceps, Substantially Equivalent on 2019-04-16. Applicant: STERIS Corporation.
Clearance details
- Applicant
- STERIS Corporation
- Product code
- Code KGE
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mentor, OH, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.