VERIFY ASSERT STEAM Process Challenge Device— 510(k) K162945
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K162945 for VERIFY ASSERT STEAM Process Challenge Device, Substantially Equivalent on 2017-04-28. Applicant: STERIS Corporation. Device class: 2.
Clearance details
- Applicant
- STERIS Corporation
- Product code
- Code OWP
- Device class
- Class 2
- Regulation
- 21 CFR 880.2805
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mentor, OH, US
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