510(k) K840702

SECURE W/25MM DIAM. SHEATH & ADHESIVE by Warne Surgical Products, Ltd. — Product Code KNX

K840702 is an FDA 510(k) premarket notification submitted by Warne Surgical Products, Ltd. for the device "SECURE W/25MM DIAM. SHEATH & ADHESIVE". The FDA issued a decision of Substantially Equivalent on March 22, 1984. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Warne Surgical Products, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 22, 1984
Date Received
February 17, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Collector, Urine, (And Accessories) For Indwelling Catheter
Device Class
Class II
Regulation Number
876.5250
Review Panel
GU
Submission Type