FDA Product Code
FDA Product Code LWI — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Radiology
- 21 CFR Citation
- 892.1560
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K960421 | SINUSCAN 102/SINUSPRINT | Ferguson Medical | 1997-04-16 | Traditional | PDF ↗ |
| K960044 | ULTRAMAX/MODEL NUMBER A1 | Entlab OY | 1996-08-02 | Traditional | PDF ↗ |
| K960241 | CPR GENERAL SURGERY TRAY | Custom Pack Reliability | 1996-03-22 | Traditional | PDF ↗ |
| K874081 | ENTERSCAN | Pie Data Medical BV | 1987-12-31 | Traditional | PDF ↗ |
Product code LWI · Class II · Radiology. Data: openFDA.