• 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 K961622
Device Name PHONAK PICONET2 P2 AZ
Applicant
PHONAK, INC.
850 E. DIEHL RD.
BOX 3117
NAPERVILLE,  IL  60566
Applicant Contact FRANCIS K KUK, PH.D.,CCC-A
Correspondent
PHONAK, INC.
850 E. DIEHL RD.
BOX 3117
NAPERVILLE,  IL  60566
Correspondent Contact FRANCIS K KUK, PH.D.,CCC-A
Regulation Number874.3300
Classification Product Code
ESD  
Date Received04/26/1996
Decision Date 05/17/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ear Nose & Throat
510k Review Panel Ear Nose & Throat
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-