HJE
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Lamp, Fluorescein, Ac-Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4580
- Medical specialty
- General, Plastic Surgery
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| VALTRAC(R) INTRODUCER FORCEP (K922348) | American Cyanamid Co. | 1992-06-09 |
| FLUORESCENT SUN LAMP FIXTURE (K802291) | Strato-Ray Co. | 1980-10-31 |
| EXAMINER 10 (K781698) | American Sterilizer Co. | 1978-11-03 |
Track HJE automatically
Every clearance here is in the API, with alerts when new ones post.