CELERITY 20 Steam Process Challenge Device for Gravity Cycles— 510(k) K173629
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K173629 for CELERITY 20 Steam Process Challenge Device for Gravity Cycles, Substantially Equivalent on 2018-02-21. Applicant: STERIS Corporation.
Clearance details
- Applicant
- STERIS Corporation
- Product code
- Code FRC
- Advisory panel
- General Hospital
- 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.