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 Dislodger, Stone, Basket, Ureteral, Metal
510(k) Number K896992
Device Name METAL URETERAL BASKET STONE DISLODGER
Applicant
Annex Medical, Inc.
7887 Fuller Rd. #109
Eden Prairie,  MN  55344
Applicant Contact STUART J LIND
Correspondent
Annex Medical, Inc.
7887 Fuller Rd. #109
Eden Prairie,  MN  55344
Correspondent Contact STUART J LIND
Regulation Number876.4680
Classification Product Code
FFL  
Date Received12/11/1989
Decision Date 02/08/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-