510(k) K931459

KENGUARD URINARY DRAINAGE BAG W/ANTIREFLUX CHAMBER by Kendall Healthcare Products Co. Div.Of Tyco Health — Product Code KNX

K931459 is an FDA 510(k) premarket notification submitted by Kendall Healthcare Products Co. Div.Of Tyco Health for the device "KENGUARD URINARY DRAINAGE BAG W/ANTIREFLUX CHAMBER". The FDA issued a decision of Substantially Equivalent on June 14, 1993. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Kendall Healthcare Products Co. Div.Of Tyco Health has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 14, 1993
Date Received
March 23, 1993
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