CMS IV Extension Sets

FDA 510(k) K884370 · Churchill Medical Systems, Inc.

Substantially Equivalent

510(k) numberK884370

Submission

Device name
CMS IV Extension Sets
Applicant
Churchill Medical Systems, Inc.
Horsham, PA, US
Received
October 18, 1988
Decision date
November 7, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPK – Tubing, Fluid Delivery
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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K063239Lifeshield Latex-Free Gravitech Flow Controller I.V. Sets, Models 17528, 17527, 17525 &…FPK · Traditional Hospira, Inc.12/11/2006SE
K052431Medtronic Minimed Leapfrog II Infusion Set, Models MMT-801S1, MMT-801L1, MMT-801S2…FPK · Traditional Medtronic Minimed11/29/2005SE
K041178Empower Transfer Set, (Cat. No. 7725)FPK · Traditional E-Z-Em, Inc.07/16/2004SE
K031808Medrad Swabbable Valve Transfer SetFPK · Special Medrad, Inc.07/11/2003SE
K022431Medrad Transfer SetFPK · Traditional Medrad, Inc.09/05/2002SE
K965208Polyfin Extension Set, Models 126 and 128FPK · Traditional Medtronic Minimed02/26/1997SE
K953864Silclear Tubing (Modification)FPK · Traditional Degania Silicone , Ltd.11/06/1995SE
K950508Sysmex SF-3000FPK · Traditional Sysmex Corp.11/03/1995SE

More from Sysmex Corp.

510(k)DeviceDecision
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K021395Modification to 30 Extension SetFPA · Special 05/13/2002SE
K013949Universal Vial Access Spike with Needleless ConnectorFPA · Traditional 03/27/2002SE
K020544Wing Safe Infusion Set 20 Ga, SHS2000 Series; Wing Safe Infusion Set 19 Ga, SHS1900…FPA · Special 03/12/2002SE
K013950Vented Vial Access DeviceFPA · Traditional 01/10/2002SE
K012157Churchill Medical Systems StopcockFMG · Traditional 09/11/2001SE
K011888Pressure Activated Check ValveFPA · Traditional 09/10/2001SE
K011336Primary Solution Set with Universal Spike, Injection Site and Male Luer LockFPA · Traditional 06/12/2001SE
K896333CMS IV FiltersFPB · Traditional 01/11/1990SE
K894954.22 & 1.2 Micron IV FiltersFPB · Traditional 11/13/1989SE

Questions and answers

When was CMS IV Extension Sets cleared by the FDA?

CMS IV Extension Sets (K884370) received a 510(k) decision of Substantially Equivalent on November 7, 1988, 20 days after the submission was received.

What is the product code of K884370?

The FDA product code is FPK – Tubing, Fluid Delivery, a Class II (moderate risk) device regulated under 21 CFR 880.5440.