Celerity Incubator— 510(k) K250061
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K250061 for Celerity Incubator, Substantially Equivalent on 2025-02-06. 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
- Special
- Location
- Mentor, OH, US
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