510(k) K890039

KLEEN TEST BASIN SET by Kleen Test Products — Product Code JOL

K890039 is an FDA 510(k) premarket notification submitted by Kleen Test Products for the device "KLEEN TEST BASIN SET". The FDA issued a decision of Substantially Equivalent on October 24, 1989. The device falls under product code JOL (Catheter And Tip, Suction), a Class II device regulated under 21 CFR 880.6740. Kleen Test Products has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 24, 1989
Date Received
January 10, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Catheter And Tip, Suction
Device Class
Class II
Regulation Number
880.6740
Review Panel
HO
Submission Type