Argosy Electronics

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
24
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K974242ARGOSY PROGRAMMABLE ONQUEJanuary 20, 1998
K971699ARGOSY DYNAMEQJuly 3, 1997
K961729ARGOSY PROGRAMMABLEMay 29, 1996
K954038K-AMP 16, HI-BAND K-AMP, ULTRA COMPRESSION & HEARING PROTECTION/HEARING INSTRUMENTSeptember 18, 1995
K952451CLASS D LINEAR WITH ACTIVE TONE CONTROLJuly 6, 1995
K952452OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROLJuly 6, 1995
K952450WIDE DYNAMIC RANGE COMPRESSION WITH ACTIVE TONE CONTROLJuly 6, 1995
K952454EXPANDER WITH ACTIVE TONE CONTROLJune 21, 1995
K952453INPUT COMPRSSION LIMITER WITH ACTIVE TONE CONTROLJune 21, 1995
K952455IMPROVED MANHATTAN IIJune 21, 1995
K944078PROGRAM 3-CH SER HEAR AIDS W/PROGRAM FIT SYST/PRO FITOctober 21, 1994
K944077PROGRAM 3-CH SERIES HEAR AIDS W/DT-1 DESKTOP PROGRAMOctober 12, 1994
K940116COMPLETELY IN THE CANALMay 3, 1994
K934452HI BANDOctober 13, 1993
K934454MANHATTAN IIOctober 8, 1993
K9344432:1 INPUT COMPRESSIONOctober 8, 1993
K9344493-CHANNEL K-AMPOctober 8, 1993
K934444K-AMPOctober 8, 1993
K934447LINEAR PLUS-POWEROctober 8, 1993
K934446POWER MANHATTAN IIOctober 8, 1993