Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name hearing aid, air-conduction, prescription
510(k) Number K935791
Device Name PHONAK PICONET 232X-AZ BTE HEARING INSTRUMENT
Applicant
PHONAK, INC.
850 E. DIEHL RD.
P.O. BOX 3017
NAPERVILLE,  IL  60566
Applicant Contact BILL LESIECKI
Correspondent
PHONAK, INC.
850 E. DIEHL RD.
P.O. BOX 3017
NAPERVILLE,  IL  60566
Correspondent Contact BILL LESIECKI
Regulation Number874.3300
Classification Product Code
ESD  
Date Received12/07/1993
Decision Date 01/26/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-