510(k) K840146

EXP* 700 PARALLEL PLATE DIALYZER by Extracorporeal Medical Specialities, Inc. — Product Code KOC

K840146 is an FDA 510(k) premarket notification submitted by Extracorporeal Medical Specialities, Inc. for the device "EXP* 700 PARALLEL PLATE DIALYZER". The FDA issued a decision of Substantially Equivalent on February 4, 1984. The device falls under product code KOC (Accessories, Blood Circuit, Hemodialysis), a Class II device regulated under 21 CFR 876.5820. Extracorporeal Medical Specialities, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 4, 1984
Date Received
January 13, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessories, Blood Circuit, Hemodialysis
Device Class
Class II
Regulation Number
876.5820
Review Panel
GU
Submission Type