Laser Media
Laser Media holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1987.
Top product codes for Laser Media
Recent clearances by Laser Media
- K872352 — FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA
- K872351 — FIBERLASE II ND:YAG LASER FOR PULMONARY USE
- K872350 — FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE
- K872031 — UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEM
- K863428 — SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAG
- K863583 — CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER
- K862444 — FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA
- K860063 — ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEM
- K855197 — FIBERLASE 100 ND: YAG MEDICAL LASER SYSTEM
- K852798 — FIBERLASE 100 MEDICAL LASER SYSTEM
- K850509 — ND:YAG FIBERLASE 100 MEDICAL LASER SYSTEM
- K844869 — FIBERLASE 100 MEDICAL LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.