The following data is part of a premarket notification filed by Bernafon-maico, Inc. with the FDA for Maico Ma42.
Device ID | K982723 |
510k Number | K982723 |
Device Name: | MAICO MA42 |
Classification | Audiometer |
Applicant | BERNAFON-MAICO, INC. 9675 WEST 76TH ST. Eden Prairie, MN 55344 |
Contact | Scott Savre |
Correspondent | Scott Savre BERNAFON-MAICO, INC. 9675 WEST 76TH ST. Eden Prairie, MN 55344 |
Product Code | EWO |
CFR Regulation Number | 874.1050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-08-05 |
Decision Date | 1998-10-28 |