The following data is part of a premarket notification filed by Steris Corporation with the FDA for Reliance Eps Endoscope Processing System And Reliance Dg Dry Germicide.
| Device ID | K220361 |
| 510k Number | K220361 |
| Device Name: | Reliance EPS Endoscope Processing System And Reliance DG Dry Germicide |
| Classification | Accessories, Germicide, Cleaning, For Endoscopes |
| Applicant | STERIS Corporation 5960 Heisley Road Mentor, OH 44060 |
| Contact | Jennifer Nalepka |
| Correspondent | Jennifer Nalepka STERIS Corporation 5960 Heisley Road Mentor, OH 44060 |
| Product Code | NZA |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-02-08 |
| Decision Date | 2022-03-10 |