The following data is part of a premarket notification filed by Steris Corporation with the FDA for Pro-lite Sterilization Trays.
| Device ID | K172755 |
| 510k Number | K172755 |
| Device Name: | PRO-LITE Sterilization Trays |
| Classification | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Applicant | Steris Corporation 5960 Heisley Road Mentor, OH 44060 |
| Contact | Tricia Cregger |
| Correspondent | Tony Piotrkowski Steris Corporation 5960 Heisley Road Mentor, OH 44060 |
| Product Code | KCT |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-12 |
| Decision Date | 2018-02-09 |
| Summary: | summary |