JAO
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Scanner, Fluorescent
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 892.1220
- Medical specialty
- Radiology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| L-LINEX-RAY FLUORESCENCE (K911749) | Montifore Medical Center | 1991-08-20 |
| ABIOMED BODY LEAD ANALYZER MODEL 200/20 (K900574) | Abiomed, Inc. | 1990-03-15 |
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Every clearance here is in the API, with alerts when new ones post.