LDY
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Fixative, Formalin-Containing
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 864.4010
- Medical specialty
- Pathology
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| DIACYTE FIXATIVE SOLUTION (K880549) | Cytocorp, Inc. | 1988-04-01 |
Track LDY automatically
Every clearance here is in the API, with alerts when new ones post.