Target Therapeutics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Target Therapeutics - FDA 510(k) Cleared Devices
70
Total
70
Cleared
0
Denied
Target Therapeutics has 70 FDA 510(k) cleared cardiovascular devices. Based in Los Angeles, US.
Historical record: 70 cleared submissions from 1985 to 1998.
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 - Target Therapeutics
70 devices
Cleared
Apr 21, 1998
DETACHABLE SILICONE BALLOON (DSB)
Neurology
529d
Cleared
Apr 21, 1998
DETACHABLE SLICONE BALLOON (DSB)
Neurology
488d
Cleared
Oct 31, 1997
RETRIEVER II
Cardiovascular
374d
Cleared
Jul 14, 1997
GUGLIELMI DETACHABLE COIL (GDC), FIBERED PLATINUM COIL, .035 TYPE, BERENSTEIN...
Neurology
90d
Cleared
Mar 24, 1997
SPINNAKER
Cardiovascular
90d
Cleared
Feb 26, 1997
BERENSTEIN COIL
Cardiovascular
134d
Cleared
Dec 17, 1996
GDC PATIENT RETURN ELECTTRODE MODEL 45021
Neurology
117d
Cleared
Sep 20, 1996
GUGLIELMI DETACHABLE COIL
Neurology
85d
Cleared
Aug 15, 1996
BERENSTEIN COIL
Neurology
90d
Cleared
May 21, 1996
GUGLIELMI DETACHABLE COIL
Neurology
90d
Cleared
May 02, 1996
TURBO TRACKER
Cardiovascular
64d
Cleared
Feb 06, 1996
FIBERED PLATINUM COIL, .035 TYPE
Cardiovascular
82d
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