510(k) K935791

PHONAK PICONET 232X-AZ BTE HEARING INSTRUMENT by Phonak, Inc. — Product Code ESD

K935791 is an FDA 510(k) premarket notification submitted by Phonak, Inc. for the device "PHONAK PICONET 232X-AZ BTE HEARING INSTRUMENT". The FDA issued a decision of Substantially Equivalent on January 26, 1994. The device falls under product code ESD (Hearing Aid, Air-Conduction, Prescription), a Class I device regulated under 21 CFR 874.3300. Phonak, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 26, 1994
Date Received
December 7, 1993
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.