OVY
- Product code
- OVY
- Device name
- Liquid Chemical Processing System
- Device class
- Class 2
- 21 CFR
- 21 CFR 880.6887
- Medical specialty
- General Hospital
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 2
- Summaries archived here
- 2 (direct download)
- 510(k) clearances (all years, FDA)
- 4 (all years; only the last 3 years are listed here)
FDA classification definition
The liquid chemical processing system is intended as a standard method for routine monitoring.
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K233682 | 2023-12-15 | STERIS Corporation | VERIFY SPORE TEST STRIP for S40 STERILANT CONCENTRAT | |
| K231746 | 2023-09-11 | STERIS Corporation | VERIFY Spore Test Strip for S40 Sterilant Concentrat |
Official FDA classification page: OVY
Classification and pathway per current FDA publications. Data from openFDA (CC0).