Fraser Harlake, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Fraser Harlake, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1981 to 1984. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Fraser Harlake, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fraser Harlake, Inc.
9 devices
Cleared
Jun 14, 1984
FRASER HARLAKE EMERG. CARE SUCTION SYS
General & Plastic Surgery
38d
Cleared
May 14, 1984
SPHYGOMANO METER
Cardiovascular
195d
Cleared
Apr 24, 1984
FRASER HARLAKE HOPE III RESUSCITATOR
Anesthesiology
14d
Cleared
Nov 29, 1983
FRASER HARLAKE DENTAL ANTI-POLUTION SYS
Anesthesiology
42d
Cleared
Nov 14, 1983
BOYLE SYSTEM ANESTHESIA GAS MACHINE
Anesthesiology
60d
Cleared
Jul 07, 1983
CYPRANE TEC 4 CONTINUOUS FLOW VAPOR.
Anesthesiology
65d
Cleared
Aug 19, 1982
POWERED EMERGENCY VENTILATOR
Anesthesiology
38d
Cleared
Jun 25, 1982
FRASER HARLAKE NITRONOX SCAVENGER
Anesthesiology
11d
Cleared
Jan 15, 1981
POSITIVE END EXPIRATORY PRESSURE VALVE
Anesthesiology
57d