LWI — Ultrasound, Sinus Class II
FDA Device Classification
Classification Details
- Product Code
- LWI
- Device Class
- Class II
- Regulation Number
- 892.1560
- Submission Type
- Review Panel
- EN
- Medical Specialty
- Radiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K960421 | ferguson medical | SINUSCAN 102/SINUSPRINT | April 16, 1997 |
| K960044 | entlab | ULTRAMAX/MODEL NUMBER A1 | August 2, 1996 |
| K960241 | custom pack reliability | CPR GENERAL SURGERY TRAY | March 22, 1996 |
| K874081 | pie data medical | ENTERSCAN | December 31, 1987 |