Millar Instruments, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Millar Instruments, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Millar Instruments, Inc. has 18 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 18 cleared submissions from 1979 to 2011.
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 - Millar Instruments, Inc.
18 devices
Cleared
Oct 18, 2011
CARDIA-CATH
Cardiovascular
67d
Cleared
Jan 05, 2010
MIKRO-CATH, MODEL 825-0101
Cardiovascular
96d
Cleared
Jul 02, 2002
MILLAR PRESSURE CONTROL UNIT MODEL PCU-2000
Cardiovascular
280d
Cleared
Mar 01, 2000
MIKRO-TIP ANGIOGRAPHIC CATHETER
Cardiovascular
120d
Cleared
Nov 07, 1995
MIKRO-TIP ANGIOGRAPHIC CATHETER
Cardiovascular
144d
Cleared
Aug 05, 1994
FLOW DIRECTED MIKRO-TIP PRESSURE TRANSDUCER
Cardiovascular
282d
Cleared
Apr 20, 1992
MILLAR NONMAGNECTIC MIKRO-TIP CATHETER PRESS. TRAN
Cardiovascular
118d
Cleared
Jan 24, 1990
MILLAR MIKRO-TIP DOPPLER CATHETER
Cardiovascular
85d
Cleared
Dec 07, 1989
MILLAR MIKRO-TIP PULSE TRANSDUCER
Cardiovascular
73d
Cleared
Nov 18, 1988
MILLAR MIKRO-TIP CATHETER PRESSURE TRANSDUCER
Cardiovascular
84d
Cleared
Jul 29, 1986
MILLAR PULSED DOPPLER VELOCIMETER
Cardiovascular
148d
Cleared
Oct 29, 1985
MILLAR MIKRO-TIP DOPPLER CATHETER
Cardiovascular
95d