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Interspec, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K940671INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND FLOWMETERNovember 22, 1994
K924231INTERSPEC APOGEE CLAJune 14, 1993
K915696INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDENovember 24, 1992
K920678ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETERApril 2, 1992
K911073PROBE REFILL KITJune 6, 1991
K910049INTERSPEC APOGEE, MODIFICATIONApril 29, 1991
K903839INTERSPEC APOGEENovember 16, 1990
K900155INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLEROctober 5, 1990
K892944INTERSPEC TRANSESOPHAGEAL PROBE MODEL 4515July 19, 1989
K890173INTERSPEC APOGEEApril 14, 1989
K863372SM-20 CARDIOSCAN DOPPLER OPTION WITH CFM700 PROBESNovember 4, 1986
K862913CARDIOSCAN WITH DOPPLER OPTIONNovember 4, 1986
K860568ULTRASONIC IMAGING SYSTEM (MODIFIED)August 11, 1986
K860579CARDIOSCAN DOPPLER OPTIONJune 30, 1986
K841263CARDIOSCAN - TM BEING APPLIED FOROctober 19, 1984
K841110NEUROTRACApril 30, 1984
K823116NEUROTRACDecember 7, 1982