The following data is part of a premarket notification filed by Phonic Ear, Inc. with the FDA for Infrared Group Amplification System, Infrared Emitter, Infrared Body Worn Receiver, Infrared Headset Receiver-stereo, It.
| Device ID | K974658 |
| 510k Number | K974658 |
| Device Name: | INFRARED GROUP AMPLIFICATION SYSTEM, INFRARED EMITTER, INFRARED BODY WORN RECEIVER, INFRARED HEADSET RECEIVER-STEREO, IT |
| 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 | 1997-12-15 |
| Decision Date | 1998-02-25 |
| Summary: | summary |