Camino Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Camino Laboratories, Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Camino Laboratories, Inc. has 18 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Historical record: 18 cleared submissions from 1982 to 1995. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Camino Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Camino Laboratories, Inc.
18 devices
Cleared
Mar 30, 1995
CAMINO VENTRICULAR DRAINAGE SYSTEM
Neurology
660d
Cleared
Apr 15, 1993
CAMINO VENTRICULAR TRANSDUCER ACCESSORY
Neurology
90d
Cleared
Apr 15, 1993
CAMINO VENTRICULAR ACCESS DEVICE
Neurology
90d
Cleared
May 01, 1992
CAMINO VENTRICULAR NEEDLE
Neurology
114d
Cleared
Jan 17, 1992
VENTRICULAR PRESSURE MONITORING KIT, MODEL 110-4HM
Neurology
88d
Cleared
Sep 23, 1991
CAMINO MODEL M420: MONIT INTER W/MEAN PRES DISPLAY
Cardiovascular
89d
Cleared
Jul 14, 1989
MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM
Cardiovascular
77d
Cleared
May 04, 1988
VENTRICULAR BOLT PRESSURE MONITORING KIT #110-4H
Neurology
44d
Cleared
May 27, 1987
CAMINO COMPARTMENTAL PRESS MONITOR CATH/110-4D
Cardiovascular
225d
Cleared
Aug 12, 1986
CAMINO CSF DRAINAGE SYSTEM MODEL 040
Neurology
84d
Cleared
Jul 18, 1986
CAMINO HAND DRILL - MODEL 030
Neurology
42d
Cleared
Feb 20, 1986
INTRACRANIAL PRESSURE MONITORING KIT 070
Neurology
156d