Medical Research Laboratories, Inc. - FDA 510(k) Cleared Devices
19
Total
15
Cleared
0
Denied
Medical Research Laboratories, Inc. has 15 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 15 cleared submissions from 1981 to 2002.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
19 devices
Cleared
Jun 26, 2002
JUMP START, MODEL 970300
Cardiovascular
76d
Cleared
Jan 23, 2002
PORTABLE INTENSIVE CARE UNIT
Cardiovascular
159d
Cleared
Sep 24, 2001
PORTABLE INTENSIVE CARE UNIT
Cardiovascular
88d
Cleared
Jun 14, 2001
PORTABLE INSTENSIVE CARE UNIT
Cardiovascular
142d
Cleared
Dec 06, 2000
AEDEFIBRILLATOR
Cardiovascular
135d
Cleared
Apr 27, 2000
PORTABLE INTENSIVE CARE UNIT, MODEL PIC
Anesthesiology
56d
Cleared
Nov 20, 1998
MODIFICATION TO PORTABLE INTENSIVE CARE UNIT
Cardiovascular
60d
Cleared
Mar 02, 1998
PORTABLE INTENSIVE CARE UNIT
Cardiovascular
130d
Cleared
Jun 05, 1995
DPD DEFIBRILLATOR
Cardiovascular
33d
Cleared
Dec 22, 1994
360 SLX ADVISORY DEFIBRILLATOR
Cardiovascular
374d
Cleared
Jun 25, 1993
DPD DEFIBRILLATOR
Cardiovascular
142d
Cleared
Jun 06, 1989
MODIFIED MRL NEUROPROBE SYSTEM V
Neurology
197d
Cleared
May 23, 1989
MRL BLOOD PRESSURE MONITOR
Cardiovascular
158d
Cleared
Dec 16, 1988
MRL PACETTE, 450SLL
Cardiovascular
284d
Cleared
Sep 16, 1988
MRL OXIMETER
Anesthesiology
81d
Cleared
Jan 28, 1988
450SLL DEFIBRILLATOR
Cardiovascular
105d
Cleared
Jun 11, 1984
PORTA PAK 90
Cardiovascular
104d
Cleared
Jan 11, 1984
PORTA PULSE III #D320
Cardiovascular
77d
Cleared
Mar 20, 1981
TRANSCUTANEOUS ELECT. NERVE STIMULATOR
Neurology
87d