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. Device class: 2.
Clearance details
- Applicant
- STERIS Corporation
- Product code
- Code FRC
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mentor, OH, US
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