The following data is part of a premarket notification filed by Magnatone Hearing Aid Corp. with the FDA for Interton Bte Hear Aid, Supra, Suprema, Minetta.
Device ID | K890525 |
510k Number | K890525 |
Device Name: | INTERTON BTE HEAR AID, SUPRA, SUPREMA, MINETTA |
Classification | Hearing Aid, Air Conduction |
Applicant | MAGNATONE HEARING AID CORP. 170 N. CYPRESS WAY P.O. BOX 180964 Casselberry, FL 32718 -0964 |
Contact | Anthony F Quick |
Correspondent | Anthony F Quick MAGNATONE HEARING AID CORP. 170 N. CYPRESS WAY P.O. BOX 180964 Casselberry, FL 32718 -0964 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-02-02 |
Decision Date | 1989-05-19 |