Henley Intl.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
44
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K943449NEUROLOGICAL DIAGNOSTIC DEVICESNovember 15, 1995
K926278STAIR CLIMBERMay 5, 1994
K926279UPPER BODY EXERCISERMay 5, 1994
K926287EXERCISE BICYCLEMarch 22, 1994
K926314HYDRA FITNESS MODEL 311 TOTAL POWERMarch 18, 1994
K926313COMPUTERIZED TESTING AND EXERCISE SYSTEMSFebruary 4, 1994
K915864MONOTRODE CUTANEOUS ELECTRODEJuly 21, 1993
K922036SONOPULS 591June 29, 1993
K926316TRUE-TRAC, STRATUSMarch 24, 1993
K920983SONOPULS 590March 9, 1993
K921828TEAM-MC IISeptember 22, 1992
K922020ENDOMED 582September 22, 1992
K904377ELECTROCONDUCTIVE MEDIANovember 15, 1991
K905672TEAM-MCOctober 15, 1991
K896817MODEL T11 FLUIDOTHERAPY UNITJanuary 18, 1991
K903828SYNAPS (TM)January 18, 1991
K900189CURAPULS 403 DIATHERMY UNITSeptember 18, 1990
K901630CHEMPAD(TM), ELECTROCONDUCTIVE MEDIA (882.1275)July 16, 1990
K896620NEUROTENSApril 26, 1990
K900419CRYOTRON-UL30February 27, 1990