Model 6100 Ambulatory Infusion System

FDA 510(k) K943310 · Pharmacia Deltec, Inc.

Substantially Equivalent - Subject to Tracking Reg.

510(k) numberK943310

Submission

Device name
Model 6100 Ambulatory Infusion System
Applicant
Pharmacia Deltec, Inc.
St. Paul, MN, US
Received
July 11, 1994
Decision date
February 21, 1995
Decision
Substantially Equivalent - Subject to Tracking Reg. (ST)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
MEA – Pump, Infusion, Pca
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5725
Specialty
General Hospital

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More from Hospira, Inc.

510(k)DeviceDecision
K942046Pharmacia Deltec Extension Set with Anti-Siphon ValveFPA · Traditional 10/04/1994SE
K942161LockboxFRN · Traditional 08/02/1994ST
K942024Port-A-Cath Low Profile Implantable Venous Access SystemLJT · Traditional 07/26/1994SE
K941445Extension Set with Anti-Siphon ValveFPA · Traditional 06/29/1994SE
K931073Cath-FinderFOZ · Traditional 05/05/1994SE
K932464Peripherallyinsrted Venous Cath. Alternate Cath.LJS · Traditional 05/02/1994SESK
K932433Pheripherally Inserted Venous Catheter-Y SiteLJS · Traditional 05/02/1994SESK
K932430Dual Lumen Peripherally Inserted Venous CatheterLJS · Traditional 05/02/1994SESK
K932211Procedural Tray for Peripherally Inserted VenousLJS · Traditional 05/02/1994SE
K932198Pharmacia Deltec Peripherally Inserted Venous CathLJS · Traditional 05/02/1994SESK

Questions and answers

When was Model 6100 Ambulatory Infusion System cleared by the FDA?

Model 6100 Ambulatory Infusion System (K943310) received a 510(k) decision of Substantially Equivalent - Subject to Tracking Reg. on February 21, 1995, 225 days after the submission was received.

What is the product code of K943310?

The FDA product code is MEA – Pump, Infusion, Pca, a Class II (moderate risk) device regulated under 21 CFR 880.5725.