Sonicaid, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K873673BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONALFebruary 26, 1988
K8720745 MHZ TRANSDUCERAugust 25, 1987
K863803VASOPULSE(TM)/MODEL 5000May 6, 1987
K862720VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBESNovember 17, 1986
K861237VASOVIEW DUPLEX IMAGING SYSTEMJuly 14, 1986
K851102VASOSCREEN IMPEDANCE PLETHYSMOGRAPHMay 16, 1985
K833902VASOSCANJanuary 27, 1984
K832374PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPHDecember 1, 1983
K833488SONICOMPNovember 28, 1983
K833227SONICAID MODEL D206E AIR EMBOLI-DETECTOctober 27, 1983
K831371MODEL FM5June 30, 1983
K812256MODEL AP 180 MINI-MONITOROctober 20, 1981
K803246ULTRASONIC STETHOSCOPEJanuary 28, 1981
K800859FETAL HEART DETECTOR #D206May 14, 1980
K800858FETAL HEART DETECTOR #'S D102 & D102RMay 14, 1980
K790678INTRAUTERINE CATHETER TIPMay 11, 1979
K780487FETAL MONITORING SYSTEMMay 9, 1978
K771379FETAL MONITORING SYS. MODEL FM3RAugust 3, 1977