The following data is part of a premarket notification filed by Oticon Corp. with the FDA for Custom Ite Hearing Aid Model: H.
Device ID | K902352 |
510k Number | K902352 |
Device Name: | CUSTOM ITE HEARING AID MODEL: H |
Classification | Hearing Aid, Air Conduction |
Applicant | OTICON CORP. 29 SCHOOLHOUSE RD. P.O. BOX 6724 Somerset, NJ 08873 |
Contact | Preben Brunved |
Correspondent | Preben Brunved OTICON CORP. 29 SCHOOLHOUSE RD. P.O. BOX 6724 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 | 1990-05-29 |
Decision Date | 1990-06-14 |