Lake Region Mfg., Inc.
FDA 510(k) medical device clearances.
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.