Bei Medical Systems Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bei Medical Systems Co., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Bei Medical Systems Co., Inc. has 4 FDA 510(k) cleared medical devices. Based in Hackensack, US.
Historical record: 4 cleared submissions from 1994 to 1997. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Bei Medical Systems Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bei Medical Systems Co., Inc.
4 devices
Cleared
Sep 05, 1997
AUTOMATIC ELECTRONIC HYSTEROSCOPIC INSUFFLATOR
Obstetrics & Gynecology
134d
Cleared
May 17, 1995
BEI MEDICAL SYSTEMS MG-1000HS MONOPOLAR GENERATOR
General & Plastic Surgery
93d
Cleared
Jul 19, 1994
HYSTEROSCOPE
Obstetrics & Gynecology
320d
Cleared
Mar 24, 1994
BEI MEDICAL SYSTEMS' SMOKE EVACUATOR
General Hospital
62d