The following data is part of a premarket notification filed by Steris Corporation with the FDA for Celerity 20 Hp Biological Indicator.
| Device ID | K172474 |
| 510k Number | K172474 |
| Device Name: | Celerity 20 HP Biological Indicator |
| Classification | Indicator, Biological Sterilization Process |
| Applicant | Steris Corporation 5960 Heisley Road Mentor, OH 44060 |
| Contact | Anthony Piotrkowski |
| Correspondent | Anthony Piotrkowski Steris Corporation 5960 Heisley Road Mentor, OH 44060 |
| Product Code | FRC |
| CFR Regulation Number | 880.2800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-08-15 |
| Decision Date | 2017-12-29 |
| Summary: | summary |