510(k) K802172

URIHESIVE SYSTEM by E. R. Squibb & Sons, Inc. — Product Code KNX

K802172 is an FDA 510(k) premarket notification submitted by E. R. Squibb & Sons, Inc. for the device "URIHESIVE SYSTEM". The FDA issued a decision of Substantially Equivalent on September 26, 1980. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. E. R. Squibb & Sons, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 26, 1980
Date Received
September 9, 1980
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