1998
505 FDA 510(k) clearances · PMA decision year
| Record | Firm | Date |
|---|---|---|
| OPTIGUIDE(TM) FIBER OPTIC DIFFUSER (P940010/S002) | Pinnacle Biologics, Inc. | 1998-01-09 |
| COHERENT PDL1 AND PDL2 LAMBDA PLUS PHOTODYNAMIC LASERS (P940011/S001) | Lumenis, Inc. | 1998-01-09 |
| 600 SERIES DYE MODULES (MODELS 630 AND 630 XP) AND SERIES 700 AND 800 KTP/532 AND KTP/YAG SURGICAL LASERS (P940012/S001) | American Medical Systems, Inc. | 1998-01-09 |
| PRO OSTEON IMPLANT 500 POROUS CORALLINE HYDROXYAPATITE BONE GRAFT SUBSTITUTE (P860005/S010) | Interpore Intl. | 1998-01-08 |
| GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST) (P940034/S005) | Gen-Probe, Inc. | 1998-01-07 |
Track 1998 automatically
Every clearance here is in the API, with alerts when new ones post.