Menlo Care, Inc.
Menlo Care, Inc. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1997.
Top product codes for Menlo Care, Inc.
Recent clearances by Menlo Care, Inc.
- K964447 — PICC CATHETER/MIDLINE CATHETER
- K951620 — MIDMARK MIDLINE CATHETER
- K945521 — CENTERMARK(R) PICC INSERTION TRAY LANDMARK(R) MIDLINE CATHETER PREP TRAY
- K944968 — LANDMARK MIDLINE CATHETER
- K950737 — LANDMARK MIDLINE CATHETER
- K943893 — PERCUTANEOUS GRAINAGE CATHETER
- K943143 — BILIARY STENT
- K930048 — SAFE-PICC CATHETER
- K933941 — MENLO CARE URINARY DIVERSION STENT
- K940127 — CENTERMARK SECURING WINGS
- K923394 — MENLO CARE AQUASTENT SET
- K930801 — INTROPEEL
- K931218 — INTROPEEL V
- K920828 — SAFE-PICC PERIPHERALLY INSERTED CENTRAL VENOUS CAT
- K920028 — LANDMARK MIDLINE CATHETER
- K920128 — VERSACATH MAINLINE CENTRAL VENOUS CATHETER
- K920133 — VERSACATH SELECTALUMEN INNER CATHETER
- K912358 — LANDMARK ADD-A-LUMEN CATHETER KIT
- K912165 — LANDMARK DUAL-LUMEN MIDLINE CATHETER SYSTEM
- K910565 — VERSACATH(TM) SELECTALUMEN(TM) W/CONVERSION TRAY
- K910566 — VERSACATH(TM) MULTILUMEN SYSTEM
- K910564 — VERSACATH(TM0 MAINLINE(TM) WITH INTRODUCTION TRAY
- K910799 — LANDMARK VENOUS ACCESS DEVICE
- K901374 — CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY
- K896774 — STREAMLINE VASCULAR ACCESS DEVICE
- K883980 — LANDMARK VENOUS ACCESS DRIVE (ADDITIONAL SIZES)
- K883866 — NEOSOFT UMBILICAL VESSEL CATHETER
- K884259 — MODIFIED LANDMARK VENOUS ACCESS DEVICE
- K882242 — LANDMARK(TM) VENOUS ACCESS DEVICE
- K862130 — COMFORT-SET* I.V. CATHETER PLACEMENT UNIT.
- K860474 — STREAM LINE* I.V. CATHETER PLACEMENT UNIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.