510(k) K832450

URO-TEX MALE EXTERNAL CATHETER by Sierra Laboratories, Inc. — Product Code KNX

K832450 is an FDA 510(k) premarket notification submitted by Sierra Laboratories, Inc. for the device "URO-TEX MALE EXTERNAL CATHETER". The FDA issued a decision of Substantially Equivalent on October 14, 1983. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Sierra Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 14, 1983
Date Received
July 26, 1983
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