![]() | ||||||||||||||
FDA 510(k) Applications for Medical Device Product Code "FQP"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K001223 | ACULUX | ACULUX, MODEL AX3001, AX3002 | 06/23/2000 |
K993314 | SYNTHES (USA) | SYNTHES LIGHT GUIDE | 12/06/1999 |