K233682 is an FDA 510(k) clearance for the VERIFY SPORE TEST STRIP for S40 STERILANT CONCENTRATE. This device is classified as a Liquid Chemical Processing System (Class II - Special Controls, product code OVY).
Submitted by STERIS Corporation (Mentor, US). The FDA issued a Cleared decision on December 15, 2023, 29 days after receiving the submission on November 16, 2023.
This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 880.6887. The Liquid Chemical Processing System Is Intended As A Standard Method For Routine Monitoring..
| 510(k) Number | K233682 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 16, 2023 |
| Decision Date | December 15, 2023 |
| Days to Decision | 29 days |
| Submission Type | Special |
| Review Panel | General Hospital (HO) |
| Summary | Summary PDF |
| Product Code | OVY — Liquid Chemical Processing System |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 880.6887 |
| Definition | The Liquid Chemical Processing System Is Intended As A Standard Method For Routine Monitoring. |