FDA Product Code
FDA Product Code OVY — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- General Hospital
- 21 CFR Citation
- 880.6887
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K233682 | VERIFY SPORE TEST STRIP for S40 STERILANT CONCENTRATE | STERIS Corporation | 2023-12-15 | Special | PDF ↗ |
| K231746 | VERIFY Spore Test Strip for S40 Sterilant Concentrate | STERIS Corporation | 2023-09-11 | Traditional | PDF ↗ |
| K180553 | VERIFY Spore Test Strip for S40 Sterilant | STERIS Corporation | 2018-05-29 | Traditional | PDF ↗ |
| DEN110002 | SYSTEM 1E PROCESS BIOLOGICAL MONITORING KIT | STERIS Corporation | 2012-03-30 | Post-NSE | — |
Product code OVY · Class II · General Hospital. Data: openFDA.