Instromedix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Instromedix, Inc. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
Instromedix, Inc. has 32 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 32 cleared submissions from 1977 to 1997.
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 - Instromedix, Inc.
32 devices
Cleared
Jul 23, 1997
POSEIDON CARDIAC MONITORING SYSTEM (PCMS)
Cardiovascular
261d
Cleared
Jul 18, 1997
CARDIOMAGIC 2000 SOFTWARE
Cardiovascular
283d
Cleared
Apr 08, 1996
ACCELERATED TRANSMISSION PROTOCOL
Cardiovascular
158d
Cleared
Jan 16, 1996
LIFESIGNS RECEIVING CENER 2000 TRANSTELEPHONIC RECEIVER
Cardiovascular
315d
Cleared
Nov 09, 1995
HEARTHWATCH III(TM)
Cardiovascular
366d
Cleared
Oct 31, 1995
CARDIOMAGIC(R) SOFTWARE ENHANCEMENTS
Cardiovascular
301d
Cleared
Sep 07, 1995
HEARTCARD CARDIAC EVENT MONITOR
Cardiovascular
365d
Cleared
Apr 04, 1995
CARRYALL ENHANCEMENTS
Cardiovascular
235d
Cleared
Nov 08, 1994
PRINCE
Cardiovascular
363d
Cleared
Jun 22, 1993
CARDIOMAGIC SOFTWARE
Cardiovascular
225d
Cleared
Mar 08, 1993
KING OF HEARTS SCEPTER
Cardiovascular
250d
Cleared
Feb 22, 1993
COMPRESSAR UNIVERSAL (TM) SYSTEM
Cardiovascular
97d