The following data is part of a premarket notification filed by Tso3, Inc. with the FDA for Sterizone Vp4 Sterilizer.
| Device ID | K173694 |
| 510k Number | K173694 |
| Device Name: | STERIZONE VP4 Sterilizer |
| Classification | Two Or More Sterilant Sterilizer |
| Applicant | TSO3, Inc. 2505, Rue Dalton Quebec, CA G1p 3s5 |
| Contact | Alexandre Jokci |
| Correspondent | Cynthia G. Pritchard BioTechnology Transfer, LLC 1016 Tobiano Lane Raleigh, NC 27614 |
| Product Code | PJJ |
| CFR Regulation Number | 880.6860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-01 |
| Decision Date | 2018-03-13 |
| Summary: | summary |