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
K952450WIDE DYNAMIC RANGE COMPRESSION WITH ACTIVE TONE CONTROLJuly 6, 1995
K952452OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROLJuly 6, 1995
K952451CLASS D LINEAR WITH ACTIVE TONE CONTROLJuly 6, 1995
K952454EXPANDER WITH ACTIVE TONE CONTROLJune 21, 1995
K952455IMPROVED MANHATTAN IIJune 21, 1995
K952453INPUT COMPRSSION LIMITER WITH ACTIVE TONE CONTROLJune 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
K934450MANHATTAN 3-CHANNELOctober 8, 1993
K9344493-CHANNEL K-AMPOctober 8, 1993
K934442LINEAR PLUSOctober 8, 1993
K934448POWER 3-CHANNEL-CLOCKOctober 8, 1993
K934446POWER MANHATTAN IIOctober 8, 1993