Laser Media - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Laser Media has 12 FDA 510(k) cleared medical devices. Based in Hauppauge, US.
Historical record: 12 cleared submissions from 1985 to 1987. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Laser Media Filter by specialty or product code using the sidebar.
12 devices
Cleared
Dec 30, 1987
FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA
Obstetrics & Gynecology
196d
Cleared
Dec 11, 1987
FIBERLASE II ND:YAG LASER FOR PULMONARY USE
Anesthesiology
177d
Cleared
Aug 10, 1987
FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE
Gastroenterology & Urology
54d
Cleared
Aug 04, 1987
UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEM
Gastroenterology & Urology
70d
Cleared
Dec 03, 1986
SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAG
Gastroenterology & Urology
90d
Cleared
Nov 24, 1986
CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER
Gastroenterology & Urology
76d
Cleared
Sep 25, 1986
FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA
Obstetrics & Gynecology
91d
Cleared
Feb 05, 1986
ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEM
Gastroenterology & Urology
30d
Cleared
Jan 21, 1986
FIBERLASE 100 ND: YAG MEDICAL LASER SYSTEM
Gastroenterology & Urology
26d
Cleared
Jul 29, 1985
FIBERLASE 100 MEDICAL LASER SYSTEM
Gastroenterology & Urology
28d
Cleared
Apr 08, 1985
ND:YAG FIBERLASE 100 MEDICAL LASER SYSTEM
Gastroenterology & Urology
59d
Cleared
Jan 14, 1985
FIBERLASE 100 MEDICAL LASER SYSTEM
Anesthesiology
31d