510(k) K070730

FLEX-NECK ARC CATHETER by Medigroup, Inc. — Product Code FJS

Clearance Details

Decision
SESK (Substantially Equivalent (kit))
Decision Date
July 3, 2007
Date Received
March 15, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter, Peritoneal, Long-Term Indwelling
Device Class
Class II
Regulation Number
876.5630
Review Panel
GU
Submission Type