Non-Invasive Tubing

FDA 510(k) K921450 · Specialty Medical Sales, Inc.

Substantially Equivalent

510(k) numberK921450

Submission

Device name
Non-Invasive Tubing
Applicant
Specialty Medical Sales, Inc.
Salem, NH, US
Received
March 26, 1992
Decision date
February 5, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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

Other 510(k)s with product code FPK

510(k)DeviceApplicantDecision
K131517Medrad Twist & Go High Pressure Connector TubingFPK · Special Medrad, Inc. / Bayer Medical Care, Inc.08/02/2013SE
K063114Disposable Transfer Sets with and Without Swabbable Valves And/Or Check ValvesFPK · Abbreviated Coeur, Inc.02/09/2007SE
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

Questions and answers

When was Non-Invasive Tubing cleared by the FDA?

Non-Invasive Tubing (K921450) received a 510(k) decision of Substantially Equivalent on February 5, 1993, 316 days after the submission was received.

What is the product code of K921450?

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