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 Lithotriptor, Electro-Hydraulic
510(k) Number K052135
Device Name CYBERSONICS CYBERWAND DUAL PROBE LITHOTRIPTER
Applicant
Cybersonics, Inc.
5368 Kuhl Rd.
Erie,  PA  16510
Applicant Contact WILLIAM A STOLL
Correspondent
Cybersonics, Inc.
5368 Kuhl Rd.
Erie,  PA  16510
Correspondent Contact WILLIAM A STOLL
Regulation Number876.4480
Classification Product Code
FFK  
Date Received08/05/2005
Decision Date 12/20/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
-
-