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Seamed Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K923398CPI MODEL 2215August 14, 1992
K915364CHRONOCOR VI MODEL 5012February 7, 1992
K912507CPI MODEL 2215 & SEAMED MODEL 3400September 3, 1991
K910223CPI MODEL 2215/SEAMED MODEL 3400March 19, 1991
K883930SEAMED MODEL 3300 DUAL CHAMBER PACING SYSTEM ANALYNovember 9, 1988
K872551SEAMED MODEL 3200July 31, 1987
K863903SEA MED MODEL 6000December 10, 1986
K860462SEAMED MODEL 3000August 19, 1986
K854648SEAMED MODEL 4000January 16, 1986
K852746EXTERNAL PACEMAKER TELECTRONICS TE200September 12, 1985
K851900SEA MED DDD PACING SYSTEM ANALYZERJuly 19, 1985
K850822CHRONOCOR V EXTERNAL PACER, MODEL 297AJuly 16, 1985
K843777SEAMED 4000February 1, 1985
K843807SEAMED MODEL 6000February 1, 1985
K831697TELECTRONICS MODEL 2401September 4, 1984
K831381RAPID ATRIAL PACERAugust 31, 1983
K823048SEA MED MODEL 880December 15, 1982
K820570SEAMED, #540 - SIEMENS, #146F TELECTROJune 3, 1982