Menlo Care, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
31
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K964447PICC CATHETER/MIDLINE CATHETERApril 16, 1997
K951620MIDMARK MIDLINE CATHETERApril 4, 1996
K945521CENTERMARK(R) PICC INSERTION TRAY LANDMARK(R) MIDLINE CATHETER PREP TRAYApril 6, 1995
K950737LANDMARK MIDLINE CATHETERMarch 29, 1995
K944968LANDMARK MIDLINE CATHETERMarch 29, 1995
K943893PERCUTANEOUS GRAINAGE CATHETERMarch 7, 1995
K943143BILIARY STENTFebruary 28, 1995
K930048SAFE-PICC CATHETERMay 12, 1994
K933941MENLO CARE URINARY DIVERSION STENTMarch 31, 1994
K940127CENTERMARK SECURING WINGSFebruary 9, 1994
K923394MENLO CARE AQUASTENT SETNovember 16, 1993
K930801INTROPEELSeptember 22, 1993
K931218INTROPEEL VSeptember 22, 1993
K920828SAFE-PICC PERIPHERALLY INSERTED CENTRAL VENOUS CATAugust 14, 1992
K920133VERSACATH SELECTALUMEN INNER CATHETERMarch 26, 1992
K920028LANDMARK MIDLINE CATHETERMarch 26, 1992
K920128VERSACATH MAINLINE CENTRAL VENOUS CATHETERMarch 26, 1992
K912358LANDMARK ADD-A-LUMEN CATHETER KITJanuary 2, 1992
K912165LANDMARK DUAL-LUMEN MIDLINE CATHETER SYSTEMDecember 11, 1991
K910566VERSACATH(TM) MULTILUMEN SYSTEMJune 3, 1991