The following data is part of a premarket notification filed by Phonic Ear, Inc. with the FDA for Group Auditory Trainer (group Amplification System).
| Device ID | K950730 |
| 510k Number | K950730 |
| Device Name: | GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM) |
| Classification | Hearing Aid, Group And Auditory Trainer |
| Applicant | PHONIC EAR, INC. 3880 CYPRESS DR. Petaluma, CA 94954 -7600 |
| Contact | Robert L Reinke |
| Correspondent | Robert L Reinke PHONIC EAR, INC. 3880 CYPRESS DR. Petaluma, CA 94954 -7600 |
| Product Code | EPF |
| CFR Regulation Number | 874.3320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-16 |
| Decision Date | 1995-06-30 |