Lake Region Mfg., Inc.
Lake Region Mfg., Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 2010.
Top product codes for Lake Region Mfg., Inc.
Recent clearances by Lake Region Mfg., Inc.
- K092965 — TRAILRUNNER GUIDEWIRES
- K082922 — FREEWAY AND RAILRUNNER GUIDEWIRES
- K081708 — TAXI ENDOSCOPIC GUIDEWIRE
- K080144 — MANDREL GUIDEWIRES OR M-WIRES
- K073655 — PEGASUS STEERABLE (PTCA) GUIDEWIRE
- K060454 — TITAN GUIDEWIRE
- K052347 — TITAN STEERABLE (PTCA) GUIDEWIRE
- K042338 — CORONARY PERIPHERAL AND RENAL STEERABLE GUIDEWIRE
- K041624 — PTCA STEERABLE HYDROPHILIC GUIDEWIRE
- K040825 — LAKE REGION HYDROPHILIC GUIDEWIRE
- K033758 — HYDROPHILIC GUIDEWIRE
- K022813 — STEERABLE GUIDEWIRE
- K011968 — STREERABLE PTCA GUIDEWIRE
- K011084 — MANDREL GUIDEWIRE ASSEMBLY
- K003483 — MODIFIED HYDROPHILIC COATED GUIDEWIRE (STAINLESS STEEL CORE)
- K000011 — MODIFIED HYDROPHILIC COATED GUIDEWIRE
- K971322 — CORE AND COIL ASSEMBLY GUIDEWIRE
- K981326 — LAKE REGION MANUFACTURING GUIDEWIRES
- K981667 — HYDROPHILIC COATED GUIDEWIRE
- K970376 — PTCA GUIDEWIRE
- K970994 — CORE AND COIL ASSEMBLY GUIDEWIRE
- K960718 — LRM
- K960866 — LRM PRODUCES GUIDEWIRES ON AN OEM BASIS FOR MANUFACTURERS,KIT ASSEMBLERS, AND DISTRIBUTORS.
- K935198 — GASTROENTEROLOGY AND UROLOGY GUIDEWIRE MODIFICATIONS
- K941229 — ONTRAC STEERABLE GUIDEWIRE
- K935170 — CARDIOVASCULAR AND VASCULAR GUIDEWIRE MODIFICATIONS
- K921200 — GUIDEWIRE
- K914138 — ONTRAC
- K913517 — ISOLATE INFUSION CATHETR SYSTEM
- K912877 — PROFUSE INFUSION SYSTEM
- K912878 — OPEN ENDED GUIDEWIRE
- K905639 — TORQUE HANDLE DEVICE FOR GUIDEWIRE
- K905581 — SILICONE COATED GUIDEWIRES
- K901224 — INSITE STEERABLE GUIDEWIRE
- K871882 — LAKE REGION VARIABLE STIFFNESS GUIDEWIRE (VSGW)
- K864058 — AMPLATZ MOVEABLE CORE GUIDEWIRE
- K861469 — DUTHOY STONE BASKET
- K861365 — FASICULATED NAIL
- K850827 — GUIDE, WIRE, ANGIOGRAPHIC
- K850828 — WIRE, GUIDE - MODIFICATION
- K850829 — WIRE, GUIDE, CATHETER
- K770977 — CARDIOVASCULAR SPRING GUIDES
Data sourced from openFDA. This site is unofficial and independent of the FDA.