510(k) K833139

ACUTE HEMODIALYSIS TRAYS by Intermed, Inc. — Product Code KNZ

K833139 is an FDA 510(k) premarket notification submitted by Intermed, Inc. for the device "ACUTE HEMODIALYSIS TRAYS". The FDA issued a decision of Substantially Equivalent on December 22, 1983. The device falls under product code KNZ (Accessories, A-V Shunt), a Class II device regulated under 21 CFR 876.5540. Intermed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 22, 1983
Date Received
September 14, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessories, A-V Shunt
Device Class
Class II
Regulation Number
876.5540
Review Panel
GU
Submission Type