510(k) K831433

EXTRASENSR ULTRAFILTRATION MONITOR by Extracorporeal Medical Specialities, Inc. — Product Code KOC

K831433 is an FDA 510(k) premarket notification submitted by Extracorporeal Medical Specialities, Inc. for the device "EXTRASENSR ULTRAFILTRATION MONITOR". The FDA issued a decision of Substantially Equivalent on June 2, 1983. 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
June 2, 1983
Date Received
May 4, 1983
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