510(k) K920797

HEMODIALYSIS BLOOD TUBING SET by National Medical Care, Medical Products Div., Inc. — Product Code FJK

K920797 is an FDA 510(k) premarket notification submitted by National Medical Care, Medical Products Div., Inc. for the device "HEMODIALYSIS BLOOD TUBING SET". The FDA issued a decision of Substantially Equivalent on September 21, 1992. The device falls under product code FJK (Set, Tubing, Blood, With And Without Anti-Regurgitation Valve), a Class II device regulated under 21 CFR 876.5820. National Medical Care, Medical Products Div., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 21, 1992
Date Received
February 21, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Device Class
Class II
Regulation Number
876.5820
Review Panel
GU
Submission Type