Medical Laser, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medical Laser, Inc. - FDA 510(k) Cleared Devices
8
Total
7
Cleared
0
Denied
Medical Laser, Inc. has 7 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 7 cleared submissions from 1989 to 1991. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medical Laser, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medical Laser, Inc.
8 devices
Cleared
Nov 01, 1991
LASER ENDOSCOPE DISC DECOMPRESSION KITS
General & Plastic Surgery
108d
Cleared
Oct 10, 1991
MEDILASE SEMI-RIGID INSTROD SHEATH SERIES AE1000
Gastroenterology & Urology
141d
Cleared
Sep 27, 1991
SERIES 5000 ENDOSCOPE CONSOLE MODELS 5100 AND 5200
Gastroenterology & Urology
116d
Cleared
Aug 12, 1991
MODIFIED SERIES 2100 ENDOSCOPES
Gastroenterology & Urology
91d
Cleared
Aug 07, 1990
MEDILASE SERIES 2200 ENDOSCOPE
Gastroenterology & Urology
132d
Cleared
Jun 22, 1990
MEDILASE SERIES 2100 ENDOSCOPE
Gastroenterology & Urology
115d
Cleared
May 15, 1990
MEDILASE 5010 ENDOSCOPE CONSOLE
Gastroenterology & Urology
109d
Cleared
Dec 14, 1989
MEDILASE SYSTEM 2010L LASER LITHOTRIPTOR
General & Plastic Surgery
72d