Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide— 510(k) K220361
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K220361 for Reliance EPS Endoscope Processing System and Reliance DG Dry Germicide, Substantially Equivalent on 2022-03-10. Applicant: STERIS Corporation. Device class: 2.
Clearance details
- Applicant
- STERIS Corporation
- Product code
- Code NZA
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Mentor, OH, US
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More clearances from STERIS Corporation
view allData sourced from openFDA. This site is unofficial and independent of the FDA.