The following data is part of a premarket notification filed by Maico Hearing Instruments, Inc. with the FDA for Audiometer/master Hearing Aid, Maico Model Mf7.
Device ID | K895310 |
510k Number | K895310 |
Device Name: | AUDIOMETER/MASTER HEARING AID, MAICO MODEL MF7 |
Classification | Audiometer |
Applicant | MAICO HEARING INSTRUMENTS, INC. 7375 BUSH LAKE RD. Minneapolis, MN 55439 -2029 |
Contact | Gerald Baiel |
Correspondent | Gerald Baiel MAICO HEARING INSTRUMENTS, INC. 7375 BUSH LAKE RD. Minneapolis, MN 55439 -2029 |
Product Code | EWO |
CFR Regulation Number | 874.1050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-08-29 |
Decision Date | 1990-01-23 |