510(k) K073051

MEDRAD CONTINUUM MR INFUSION SYSTEM WITH WIRELESS REMOTE ACCESSORY by Medrad, Inc. — Product Code FRN

K073051 is an FDA 510(k) premarket notification submitted by Medrad, Inc. for the device "MEDRAD CONTINUUM MR INFUSION SYSTEM WITH WIRELESS REMOTE ACCESSORY". The FDA issued a decision of Substantially Equivalent on May 30, 2008. The device falls under product code FRN (Pump, Infusion), a Class II device regulated under 21 CFR 880.5725. Medrad, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 30, 2008
Date Received
October 29, 2007
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Infusion
Device Class
Class II
Regulation Number
880.5725
Review Panel
HO
Submission Type