HJN — Transilluminator, Battery-Powered Class I
FDA Device Classification
Classification Details
- Product Code
- HJN
- Device Class
- Class I
- Regulation Number
- 886.1945
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K941035 | trinity partners | VENOSCOPE | May 16, 1994 |
| K912747 | lumitex | LULMITEX NEONATAL TRANSILLUMINATOR | December 24, 1991 |
| K901309 | sylvan | SYLVAN PEDIASCAN 200 TRANSILLUMINATOR | May 24, 1990 |