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 Catheter, Peritoneal, Long-Term Indwelling
510(k) Number K070730
Device Name FLEX-NECK ARC CATHETER
Applicant
Medigroup, Inc.
14 A Stonehill Rd.
Oswego,  IL  60543
Applicant Contact JOHN A NAVIS
Correspondent
Medigroup, Inc.
14 A Stonehill Rd.
Oswego,  IL  60543
Correspondent Contact JOHN A NAVIS
Regulation Number876.5630
Classification Product Code
FJS  
Date Received03/15/2007
Decision Date 07/03/2007
Decision Substantially Equivalent - Kit (SESK)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
-
-