CELERITY 20 HP Biological Indicator, CELERITY HP Challenge Pack— 510(k) K183294
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K183294 for CELERITY 20 HP Biological Indicator, CELERITY HP Challenge Pack, Substantially Equivalent on 2019-01-03. 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
Recent devices under product code FRC
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