Enpath Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enpath Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Enpath Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 5 cleared submissions from 2006 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Enpath Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Enpath Medical, Inc.
5 devices
Cleared
Sep 15, 2008
PTFE INTERLOCK PEELABLE INTRODUCERS
Cardiovascular
119d
Cleared
Nov 09, 2007
VIAPEEL PEELABLE INTRODUCER
Cardiovascular
88d
Cleared
Jul 05, 2007
STIFFER COAXIAL MICRO-INTRODUCER KIT
Cardiovascular
27d
Cleared
Dec 21, 2006
ENPATH MEDICAL VIASEAL VALVED PEELABLE INTRODUCER, MODEL 10866-XXX
Cardiovascular
63d
Cleared
May 18, 2006
ENPATH MEDICAL STEERABLE SHEATH
Cardiovascular
27d