The following data is part of a premarket notification filed by Phonic Ear, Inc. with the FDA for Pe 400ir, Pe 400t, Pe 400e.
| Device ID | K923234 |
| 510k Number | K923234 |
| Device Name: | PE 400IR, PE 400T, PE 400E |
| 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 | 1992-07-01 |
| Decision Date | 1992-09-29 |