The following data is part of a premarket notification filed by Phonic Ear, Inc. with the FDA for Phonic Ear Model Pe805cd.
Device ID | K813583 |
510k Number | K813583 |
Device Name: | PHONIC EAR MODEL PE805CD |
Classification | Hearing Aid, Air Conduction |
Applicant | PHONIC EAR, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1981-12-28 |
Decision Date | 1982-01-12 |