Menlo Care, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Menlo Care, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PICC CATHETER/MIDLINE CATHETER, MIDMARK MIDLINE CATHETER, CENTERMARK(R) PICC INSERTION TRAY LANDMARK(R) MIDLINE CATHETER PREP TRAY
31
Total
25
Cleared
0
Denied
Menlo Care, Inc. has 25 FDA 510(k) cleared general hospital devices. Based in Menlo Park, US.
Historical record: 25 cleared submissions from 1986 to 1997.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Menlo Care, Inc.
31 devices
Cleared
Apr 16, 1997
PICC CATHETER/MIDLINE CATHETER
General Hospital
161d
Cleared
Apr 04, 1996
MIDMARK MIDLINE CATHETER
General Hospital
363d
Cleared
Apr 06, 1995
CENTERMARK(R) PICC INSERTION TRAY LANDMARK(R) MIDLINE CATHETER PREP TRAY
General Hospital
147d
Cleared
Mar 29, 1995
LANDMARK MIDLINE CATHETER
General Hospital
169d
Cleared
Mar 29, 1995
LANDMARK MIDLINE CATHETER
General Hospital
41d
Cleared
Mar 07, 1995
PERCUTANEOUS GRAINAGE CATHETER
Gastroenterology & Urology
210d
Cleared
Feb 28, 1995
BILIARY STENT
Gastroenterology & Urology
243d
Cleared
May 12, 1994
SAFE-PICC CATHETER
General Hospital
492d
Cleared
Mar 31, 1994
MENLO CARE URINARY DIVERSION STENT
Gastroenterology & Urology
231d
Cleared
Feb 09, 1994
CENTERMARK SECURING WINGS
General Hospital
30d
Cleared
Nov 16, 1993
MENLO CARE AQUASTENT SET
Gastroenterology & Urology
494d
Cleared
Sep 22, 1993
INTROPEEL
Cardiovascular
218d