The following data is part of a premarket notification filed by Oticon, Inc. with the FDA for Oticon Digisound Compact.
Device ID | K973886 |
510k Number | K973886 |
Device Name: | OTICON DIGISOUND COMPACT |
Classification | Hearing Aid, Air Conduction |
Applicant | OTICON, INC. 29 SCHOOLHOUSE RD. Somerset, NJ 08873 |
Contact | Preben Brunved |
Correspondent | Preben Brunved OTICON, INC. 29 SCHOOLHOUSE RD. Somerset, NJ 08873 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-10-14 |
Decision Date | 1997-11-04 |