The following data is part of a premarket notification filed by Miracle-ear/dahlberg, Inc. with the FDA for Dahlberg Model Db Behind-the-ear Hearing Aid.
Device ID | K851866 |
510k Number | K851866 |
Device Name: | DAHLBERG MODEL DB BEHIND-THE-EAR HEARING AID |
Classification | Hearing Aid, Air Conduction |
Applicant | MIRACLE-EAR/DAHLBERG, INC. 7731 COUNTRY CLUB DR. Golden Valley, MN 55427 |
Contact | Jane E Hixson |
Correspondent | Jane E Hixson MIRACLE-EAR/DAHLBERG, INC. 7731 COUNTRY CLUB DR. Golden Valley, MN 55427 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-04-29 |
Decision Date | 1985-07-05 |