I-Flow Elastomeric Pump (On-Q, Painbuster, C-Block, Homepump, Easypump)

FDA 510(k) K052117 · I-Flow Corp.

Substantially Equivalent

510(k) numberK052117

Submission

Device name
I-Flow Elastomeric Pump (On-Q, Painbuster, C-Block, Homepump, Easypump)
Applicant
I-Flow Corp.
Lake Forest, CA, US
Received
August 4, 2005
Decision date
September 9, 2005
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

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

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More from Advanced Infusion, Inc.

510(k)DeviceDecision
K131249On-Q Painbuster, On-Q C-Bloc, Homepump Eclipse, Homepump C-SeriesMEB · Traditional 02/03/2014SE
K063530On-Q, Painbuster, C-Bloc, Select-A-Flow, Ondemand, Homepump, Eclipse, C-Series, One-Step…MEB · Special 01/26/2007SE
K063234On-Q IntroducersBSO · Abbreviated 11/21/2006SE
K051401On-Q Catheter, On-Antimicrobial Catheter, Soaker Catheter, I-Flow CatheterBSO · Traditional 11/30/2005SE
K043456Modification to Soaker CatheterBSO · Special 01/11/2005SE
K040337I-Flow Elastomeric Pump (On-Q, Painbuster, C-Bloc, Homepump)MEB · Traditional 05/24/2004SE
K023883Homepump, Eclipse, C-Series, Painbuster, C-Bloc, On-Q, Easypump, KvoMEB · Special 12/20/2002SE
K023827Paragon Infusion System with BolusFRN · Special 12/13/2002SE
K023318I-Flow Elastomeric Pump with BolusMEB · Special 10/18/2002SE
K022869Soaker CatheterFRN · Special 09/20/2002SE

Questions and answers

When was I-Flow Elastomeric Pump (On-Q, Painbuster, C-Block, Homepump, Easypump) cleared by the FDA?

I-Flow Elastomeric Pump (On-Q, Painbuster, C-Block, Homepump, Easypump) (K052117) received a 510(k) decision of Substantially Equivalent on September 9, 2005, 36 days after the submission was received.

What is the product code of K052117?

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