510(k) K872473

POST-AURICULAR HEARING AID MODEL PE 805CD2 by Phonic Ear, Inc. — Product Code ESD

K872473 is an FDA 510(k) premarket notification submitted by Phonic Ear, Inc. for the device "POST-AURICULAR HEARING AID MODEL PE 805CD2". The FDA issued a decision of Substantially Equivalent on July 28, 1987. The device falls under product code ESD (Hearing Aid, Air-Conduction, Prescription), a Class I device regulated under 21 CFR 874.3300. Phonic Ear, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 28, 1987
Date Received
June 23, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Hearing Aid, Air-Conduction, Prescription
Device Class
Class I
Regulation Number
874.3300
Review Panel
EN
Submission Type

An air-conduction hearing aid is a wearable sound amplifying device intended to compensate for impaired hearing that conducts sound to the ear through the air. This is a prescription hearing aid.