Lake Region Mfg., Inc. - FDA 510(k) Cleared Devices
42
Total
42
Cleared
0
Denied
Lake Region Mfg., Inc. has 42 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 42 cleared submissions from 1977 to 2010.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
42 devices
Cleared
Feb 26, 2010
TRAILRUNNER GUIDEWIRES
Cardiovascular
154d
Cleared
Dec 09, 2008
FREEWAY AND RAILRUNNER GUIDEWIRES
Cardiovascular
69d
Cleared
Aug 26, 2008
TAXI ENDOSCOPIC GUIDEWIRE
Gastroenterology & Urology
70d
Cleared
Feb 26, 2008
MANDREL GUIDEWIRES OR M-WIRES
Cardiovascular
35d
Cleared
Jan 28, 2008
PEGASUS STEERABLE (PTCA) GUIDEWIRE
Cardiovascular
33d
Cleared
Mar 24, 2006
TITAN GUIDEWIRE
Cardiovascular
30d
Cleared
Feb 17, 2006
TITAN STEERABLE (PTCA) GUIDEWIRE
Cardiovascular
172d
Cleared
Sep 16, 2004
CORONARY PERIPHERAL AND RENAL STEERABLE GUIDEWIRE
Cardiovascular
17d
Cleared
Jul 16, 2004
PTCA STEERABLE HYDROPHILIC GUIDEWIRE
Cardiovascular
30d
Cleared
May 17, 2004
LAKE REGION HYDROPHILIC GUIDEWIRE
Cardiovascular
48d
Cleared
Dec 19, 2003
HYDROPHILIC GUIDEWIRE
Cardiovascular
17d
Cleared
Feb 14, 2003
STEERABLE GUIDEWIRE
Cardiovascular
172d
Looking for a specific device from Lake Region Mfg., Inc.? Search by device name or K-number.
Search all Lake Region Mfg., Inc. devices