Aries Medical, Inc. - FDA 510(k) Cleared Devices
19
Total
18
Cleared
0
Denied
Aries Medical, Inc. has 18 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 18 cleared submissions from 1984 to 1991.
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 - Aries Medical, Inc.
19 devices
Cleared
Oct 28, 1991
SJM/CAD ISOFLOW(TM) CENTRIFUGAL PUMP 2100CP, MODIF
Cardiovascular
150d
Cleared
Dec 21, 1990
ARIES MELDICAL MODEL 2100HC HANK CRANK
Cardiovascular
130d
Cleared
Aug 23, 1990
ARIES TAPERSEAL(TM) SHEATH
Cardiovascular
23d
Cleared
Apr 10, 1990
ARIES 30CC & 50CC INTRA-AORTIC BALLOON & CONT. SYS
Cardiovascular
215d
Cleared
Dec 12, 1988
ARIES 40CC PERCU. (D/L) INTRA-AORTIC BALLOON CATH.
Cardiovascular
194d
Cleared
Jun 19, 1987
40CC PERCUTANEOUS PRE-FURL (D/L) BALLOON CATHETER
Cardiovascular
214d
Cleared
Jun 19, 1987
40CC PER. PRE-FURL (S/L) INTRA-AORTIC CATHETER
Cardiovascular
179d
Cleared
May 12, 1987
40CC PERCUTANEOUS FURL DOU. LUMEN BALLOON CATHETER
Cardiovascular
174d
Cleared
May 12, 1987
40CC SURGICAL DOUBLE LUMEN BALLOON CATHETER
Cardiovascular
174d
Cleared
Apr 22, 1987
ARIES PEEL AWAY PERCUTANEOUS CATHETER INTRODUCER
Cardiovascular
30d
Cleared
Mar 16, 1987
ARIES TAPERED SHEATH
Cardiovascular
59d
Cleared
Jan 16, 1987
40CC PERCUTANEOUS FURL SINGLE INTRA-AORTIC BALLOON
Cardiovascular
150d