510(k) K781521

CUTTER RESIFLEX URINE METER by Cutter Laboratories, Inc. — Product Code KNX

K781521 is an FDA 510(k) premarket notification submitted by Cutter Laboratories, Inc. for the device "CUTTER RESIFLEX URINE METER". The FDA issued a decision of Substantially Equivalent on November 22, 1978. The device falls under product code KNX (Collector, Urine, (And Accessories) For Indwelling Catheter), a Class II device regulated under 21 CFR 876.5250. Cutter Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 22, 1978
Date Received
September 5, 1978
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