510(k) K780134

URINARY DRAINAGE MONITORING SYSTEM by Medical Devices, Inc. — Product Code FCN

K780134 is an FDA 510(k) premarket notification submitted by Medical Devices, Inc. for the device "URINARY DRAINAGE MONITORING SYSTEM". The FDA issued a decision of Substantially Equivalent on February 2, 1978. The device falls under product code FCN (Urinary Drainage Collection Kit, For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Medical Devices, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 2, 1978
Date Received
January 24, 1978
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Urinary Drainage Collection Kit, For Indwelling Catheter
Device Class
Class II
Regulation Number
876.5250
Review Panel
GU
Submission Type