Medical Device Manufacturer · US , Chaska , MN

Lake Region Medical

15 submissions · 15 cleared · Since 2008
15
Total
15
Cleared
0
Denied

Lake Region Medical has 15 FDA 510(k) cleared cardiovascular devices. Based in Chaska, US.

Latest FDA clearance: Dec 2024. Active since 2008.

Browse the FDA 510(k) cleared devices submitted by Lake Region MedicalFilter by specialty or product code using the sidebar.

15 devices
1–12 of 15
PTFE Guidewire
K242824 · DQX Wire, Guide, Catheter · Cardiovascular
Dec 2024 79d
Pre-Formed Blue
K221575 · DQX Wire, Guide, Catheter · Cardiovascular
Oct 2022 128d
Pre-Formed Extra Support Guidewire
K211741 · DQX Wire, Guide, Catheter · Cardiovascular
Nov 2021 168d
ENROUTE 0.014 Guidewire
K160643 · DQX Wire, Guide, Catheter · Cardiovascular
Oct 2016 225d
Pre-Formed Guidewire
K151244 · DQX Wire, Guide, Catheter · Cardiovascular
Jun 2015 31d
HI TORQUE CONNECT GUIDEWIRE, HI TORQUE CONNECT FLEX GUIDEWIRE, HI TORQUE CONNECT 250T GUIDEWIRE
K140536 · DQX Wire, Guide, Catheter · Cardiovascular
Dec 2014 288d
PREDICATE III GUIDEWIRE
K142393 · DQX Wire, Guide, Catheter · Cardiovascular
Nov 2014 90d
Predicate III Guidewire
K142397 · OCY Endoscopic Guidewire, Gastroenterology-urology · Gastroenterology & Urology
Sep 2014 23d
MANDREL GUIDEWIRE
K140482 · OCY Endoscopic Guidewire, Gastroenterology-urology · Gastroenterology & Urology
Apr 2014 41d
HYDROPHILIC COATED GUIDEWIRE
K133155 · DQX Wire, Guide, Catheter · Cardiovascular
Apr 2014 172d
MANDREL GUIDEWIRE
K140485 · DQX Wire, Guide, Catheter · Cardiovascular
Mar 2014 29d
OSTAVI HYDROPHILIC GUIDEWIRE
K124052 · OCY Endoscopic Guidewire, Gastroenterology-urology · Gastroenterology & Urology
Feb 2013 57d
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