Interspec, Inc. - FDA 510(k) Cleared Devices
17
Total
16
Cleared
0
Denied
Interspec, Inc. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 16 cleared submissions from 1982 to 1994. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Interspec, Inc. Filter by specialty or product code using the sidebar.
17 devices
Cleared
Nov 22, 1994
INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND...
Radiology
279d
Cleared
Jun 14, 1993
INTERSPEC APOGEE CLA
Radiology
297d
Cleared
Nov 24, 1992
INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE
Radiology
337d
Cleared
Apr 02, 1992
ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETER
Radiology
48d
Cleared
Jun 06, 1991
PROBE REFILL KIT
Radiology
87d
Cleared
Apr 29, 1991
INTERSPEC APOGEE, MODIFICATION
Cardiovascular
112d
Cleared
Nov 16, 1990
INTERSPEC APOGEE
Cardiovascular
87d
Cleared
Oct 05, 1990
INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER
Radiology
266d
Cleared
Jul 19, 1989
INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515
Cardiovascular
89d
Cleared
Apr 14, 1989
INTERSPEC APOGEE
Radiology
87d
Cleared
Nov 04, 1986
CARDIOSCAN WITH DOPPLER OPTION
Cardiovascular
95d
Cleared
Nov 04, 1986
SM-20 CARDIOSCAN DOPPLER OPTION WITH CFM700 PROBES
Cardiovascular
63d
Cleared
Aug 11, 1986
ULTRASONIC IMAGING SYSTEM (MODIFIED)
Radiology
178d
Cleared
Jun 30, 1986
CARDIOSCAN DOPPLER OPTION
Cardiovascular
132d
Cleared
Oct 19, 1984
CARDIOSCAN - TM BEING APPLIED FOR
Cardiovascular
207d
Cleared
Apr 30, 1984
NEUROTRAC
Neurology
76d
Cleared
Dec 07, 1982
NEUROTRAC
Neurology
47d