Medivision Scope Service Center, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medivision Scope Service Center, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Medivision Scope Service Center, Inc. has 5 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Historical record: 5 cleared submissions from 1997 to 1999.
Browse the FDA 510(k) cleared devices submitted by Medivision Scope Service Center, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medivision Scope Service Center, Inc.
5 devices
Cleared
Mar 17, 1999
MEDIVISION LAPAROSCOPE
General & Plastic Surgery
93d
Cleared
Oct 07, 1998
MEDIVISION HYSTEROSCOPE
Obstetrics & Gynecology
69d
Cleared
Sep 30, 1998
MEDIVISION CYSTOSCOPE
Gastroenterology & Urology
65d
Cleared
Jul 31, 1997
MEDIVISION ARTHROSCOP
Orthopedic
62d
Cleared
Jun 26, 1997
MEDIVISION SINOSCOPE
Ear, Nose, Throat
27d