510(k) K943310

MODEL 6100 AMBULATORY INFUSION SYSTEM by Pharmacia Deltec, Inc. — Product Code MEA

K943310 is an FDA 510(k) premarket notification submitted by Pharmacia Deltec, Inc. for the device "MODEL 6100 AMBULATORY INFUSION SYSTEM". The FDA issued a decision of ST on February 21, 1995. The device falls under product code MEA (Pump, Infusion, Pca), a Class II device regulated under 21 CFR 880.5725. Pharmacia Deltec, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
ST ()
Decision Date
February 21, 1995
Date Received
July 11, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

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