The following data is part of a premarket notification filed by Argosy Electronics with the FDA for K-amp.
Device ID | K934444 |
510k Number | K934444 |
Device Name: | K-AMP |
Classification | Hearing Aid, Air Conduction |
Applicant | ARGOSY ELECTRONICS 10300 WEST 70TH ST. P.O. BOX 59072 Eden Prairie, MN 55344 |
Contact | David A Preves |
Correspondent | David A Preves ARGOSY ELECTRONICS 10300 WEST 70TH ST. P.O. BOX 59072 Eden Prairie, MN 55344 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-09-10 |
Decision Date | 1993-10-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() K-AMP 74162482 1688921 Live/Registered |
ETYMOTIC RESEARCH, INC. 1991-05-01 |
![]() K-AMP 73068493 1076320 Dead/Expired |
KENTROX INDUSTRIES, INC. 1975-11-10 |