Arco Medical Products Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arco Medical Products Co. - FDA 510(k) Cleared Devices
21
Total
20
Cleared
0
Denied
Arco Medical Products Co. has 20 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 20 cleared submissions from 1976 to 1980.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arco Medical Products Co.
21 devices
Cleared
Nov 19, 1980
MODEL 3003 UNIPOLAR DEMAND CARDIAC GEN.
Cardiovascular
30d
Cleared
Sep 09, 1980
EXTERNAL SILASTIC BOOT FOR CARDIAC PULSE
Cardiovascular
41d
Cleared
Jun 30, 1980
PROGRAMMABLE BIPOLAR CARDIAC GENERATOR
Cardiovascular
76d
Cleared
Jun 30, 1980
UNIPOLAR PROGRAMMABLE LITHIUM CARD. GEN.
Cardiovascular
34d
Cleared
Jun 04, 1980
ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN.
Cardiovascular
50d
Cleared
Mar 17, 1980
ARCOLITH 3021-CARDIAC PULSE GENERATOR
Cardiovascular
34d
Cleared
Nov 29, 1979
ARCOLITH 2100-CARDIAC PULSE GENERATOR
Cardiovascular
24d
Cleared
Nov 29, 1979
ARCOLITH 3020-CARDIAC PULSE GENERATOR
Cardiovascular
15d
Cleared
Sep 27, 1979
ARCOLITH 2000
Cardiovascular
27d
Cleared
Aug 03, 1979
ARCO PROGAMMABLE PACEMAKER SYSTEM
Cardiovascular
46d
Cleared
Jul 10, 1979
ARCOLITH 4000
Cardiovascular
15d
Cleared
May 14, 1979
IMPLANTABLE HEART LEAD TERMINAL ADAPTER
Cardiovascular
68d