Oscor Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oscor Medical Corp. - FDA 510(k) Cleared Devices
31
Total
30
Cleared
0
Denied
Oscor Medical Corp. has 30 FDA 510(k) cleared cardiovascular devices. Based in Washington, US.
Historical record: 30 cleared submissions from 1985 to 1994.
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 - Oscor Medical Corp.
31 devices
Not Cleared
Apr 01, 1997
OSCOR PERMANENT RETRACTABLE SCREW-IN PACING LEAD MODEL PR
Cardiovascular
168d
Cleared
May 03, 1994
MISCELLANEOUS PACING LEAD
Cardiovascular
567d
Cleared
May 19, 1993
EXTERNAL DEMAND PACEMAKER
Cardiovascular
302d
Cleared
Feb 04, 1992
OSCOR MEDICAL CORP PERMANENT PACING LEAD
Cardiovascular
221d
Cleared
Jan 27, 1992
PERMANENT PACING LEADS, MODIFICATION
Cardiovascular
84d
Cleared
Jan 27, 1992
PERMANENT PACING PAD, MODIFICATION
Cardiovascular
84d
Cleared
Sep 23, 1991
MODIFIED OSCOR PY PACING LEADS/MODIFICATION
Cardiovascular
77d
Cleared
Sep 23, 1991
PRODUCTS IMPLANT PACING LEAD, TINED, MODIFICATION
Cardiovascular
77d
Cleared
Sep 23, 1991
IMPLANT PACING LEAD, TINED #3262, MODIFICATION
Cardiovascular
77d
Cleared
Sep 23, 1991
IMPLANT PACING LEAD TINED #3390, MODIFICATION
Cardiovascular
77d
Cleared
Sep 23, 1991
MODEL KY PACEMAKER LEAD-VARIOUS, MODIFICATION
Cardiovascular
77d
Cleared
Sep 23, 1991
OSCOR MEDICAL FIX SCREW PAC LEAD/PEEL CATH, MODIF
Cardiovascular
77d