The following data is part of a premarket notification filed by Phonic Ear, Inc. with the FDA for Post-auricular Hearing Aid Model Pe 805 Scd2.
Device ID | K872474 |
510k Number | K872474 |
Device Name: | POST-AURICULAR HEARING AID MODEL PE 805 SCD2 |
Classification | Hearing Aid, Air Conduction |
Applicant | PHONIC EAR, INC. 250 CAMINO ALTO Mill Valley, CA 94941 |
Contact | Robert L Reinke |
Correspondent | Robert L Reinke PHONIC EAR, INC. 250 CAMINO ALTO Mill Valley, CA 94941 |
Product Code | ESD |
CFR Regulation Number | 874.3300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-06-23 |
Decision Date | 1987-07-28 |