Hospira Gemstar Infusion Pump System, Hospira Gemstar Connect Software

FDA 510(k) K042980 · Hospira, Inc.

Substantially Equivalent

510(k) numberK042980

Submission

Device name
Hospira Gemstar Infusion Pump System, Hospira Gemstar Connect Software
Applicant
Hospira, Inc.
Lake Forest, IL, US
Received
October 29, 2004
Decision date
November 17, 2004
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

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

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Questions and answers

When was Hospira Gemstar Infusion Pump System, Hospira Gemstar Connect Software cleared by the FDA?

Hospira Gemstar Infusion Pump System, Hospira Gemstar Connect Software (K042980) received a 510(k) decision of Substantially Equivalent on November 17, 2004, 19 days after the submission was received.

What is the product code of K042980?

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