Seamed Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seamed Corp. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Seamed Corp. has 18 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 18 cleared submissions from 1982 to 1992.
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 - Seamed Corp.
18 devices
Cleared
Aug 14, 1992
CPI MODEL 2215
Cardiovascular
35d
Cleared
Feb 07, 1992
CHRONOCOR VI MODEL 5012
Cardiovascular
72d
Cleared
Sep 03, 1991
CPI MODEL 2215 & SEAMED MODEL 3400
Cardiovascular
89d
Cleared
Mar 19, 1991
CPI MODEL 2215/SEAMED MODEL 3400
Cardiovascular
60d
Cleared
Nov 09, 1988
SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALY
Cardiovascular
55d
Cleared
Jul 31, 1987
SEAMED MODEL 3200
Cardiovascular
32d
Cleared
Dec 10, 1986
SEA MED MODEL 6000
Cardiovascular
64d
Cleared
Aug 19, 1986
SEAMED MODEL 3000
Cardiovascular
194d
Cleared
Jan 16, 1986
SEAMED MODEL 4000
Cardiovascular
58d
Cleared
Sep 12, 1985
EXTERNAL PACEMAKER TELECTRONICS TE200
Cardiovascular
77d
Cleared
Jul 19, 1985
SEA MED DDD PACING SYSTEM ANALYZER
Cardiovascular
80d
Cleared
Jul 16, 1985
CHRONOCOR V EXTERNAL PACER, MODEL 297A
Cardiovascular
138d
Cleared
Feb 01, 1985
SEAMED 4000
Cardiovascular
129d
Cleared
Feb 01, 1985
SEAMED MODEL 6000
Cardiovascular
127d
Cleared
Sep 04, 1984
TELECTRONICS MODEL 2401
Cardiovascular
468d
Cleared
Aug 31, 1983
RAPID ATRIAL PACER
Cardiovascular
125d
Cleared
Dec 15, 1982
SEA MED MODEL 880
Cardiovascular
61d
Cleared
Jun 03, 1982
SEAMED, #540 - SIEMENS, #146F TELECTRO
Cardiovascular
93d