510(k) K944352

SMARTDOSE III INFUSION CONTAINER by River Medical, Inc. — Product Code FRN

K944352 is an FDA 510(k) premarket notification submitted by River Medical, Inc. for the device "SMARTDOSE III INFUSION CONTAINER". The FDA issued a decision of ST on November 15, 1995. The device falls under product code FRN (Pump, Infusion), a Class II device regulated under 21 CFR 880.5725. River Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
ST ()
Decision Date
November 15, 1995
Date Received
September 6, 1994
Clearance Type
Traditional
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