The following data is part of a premarket notification filed by Electone, Inc. with the FDA for Personal Amplifier Model Ultra Helix.
| Device ID | K893433 |
| 510k Number | K893433 |
| Device Name: | PERSONAL AMPLIFIER MODEL ULTRA HELIX |
| Classification | Hearing Aid, Air Conduction |
| Applicant | ELECTONE, INC. P.O. BOX 910 Winter Park, FL 32790 |
| Contact | Minard Freant |
| Correspondent | Minard Freant ELECTONE, INC. P.O. BOX 910 Winter Park, FL 32790 |
| Product Code | ESD |
| CFR Regulation Number | 874.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-05-02 |
| Decision Date | 1989-06-14 |