510(k) K802389

GAMBRO LUNDIA PLATE DISP. DIALYZER by Gambro, Inc. — Product Code FJG

K802389 is an FDA 510(k) premarket notification submitted by Gambro, Inc. for the device "GAMBRO LUNDIA PLATE DISP. DIALYZER". The FDA issued a decision of Substantially Equivalent on December 22, 1980. The device falls under product code FJG (Dialyzer, Parallel Flow), a Class II device regulated under 21 CFR 876.5820. Gambro, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 22, 1980
Date Received
September 29, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dialyzer, Parallel Flow
Device Class
Class II
Regulation Number
876.5820
Review Panel
GU
Submission Type