510(k) K761360

8 LATEX EXTENSION TUBE WITH CONNECTOR by Intermed, Inc. — Product Code KNX

K761360 is an FDA 510(k) premarket notification submitted by Intermed, Inc. for the device "8 LATEX EXTENSION TUBE WITH CONNECTOR". The FDA issued a decision of Substantially Equivalent on January 10, 1977. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Intermed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 10, 1977
Date Received
December 30, 1976
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