The following data is part of a premarket notification filed by Maico Hearing Instruments, Inc. with the FDA for Model P20/p21 In-the-ear Hearing Aid.
Device ID | K882692 |
510k Number | K882692 |
Device Name: | MODEL P20/P21 IN-THE-EAR HEARING AID |
Classification | Hearing Aid, Air Conduction |
Applicant | MAICO HEARING INSTRUMENTS, INC. 7375 BUSH LAKE RD. Minneapolis, MN 55439 -2029 |
Contact | Duane Smedsrud |
Correspondent | Duane Smedsrud MAICO HEARING INSTRUMENTS, INC. 7375 BUSH LAKE RD. Minneapolis, MN 55439 -2029 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-06-28 |
Decision Date | 1988-07-15 |