DIY
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Gas Chromatography, Ethosuximide
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3380
- Medical specialty
- Clinical Toxicology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ANTICONVULSANTS II CALIBRATOR KIT (K780734) | Vitek Systems, Inc. | 1978-06-22 |
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Every clearance here is in the API, with alerts when new ones post.