Swan Ganz Catheters

FDA 510(k) K160084 · Edwards Lifesciences, LLC

Substantially Equivalent

510(k) numberK160084

Submission

Device name
Swan Ganz Catheters
Applicant
Edwards Lifesciences, LLC
Irvine, CA, US
Received
January 15, 2016
Decision date
May 3, 2016
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DYG – Catheter, Flow Directed
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1240
Specialty
Cardiovascular

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K094048Percupro Messenger Balloon CatheterDYG · Traditional Cardiosolutions, Inc.07/14/2011SE
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K010253Angio Flow Thermodilution Catheter, Model AF-CATH-01; Angioflow Meter, Models HQ100 and…DYG · Traditional Transonic Systems, Inc.03/19/2002SE
K012225Attain 6215 Venogram Balloon CatheterDYG · Traditional Medtronic Vascular08/28/2001SE

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Questions and answers

When was Swan Ganz Catheters cleared by the FDA?

Swan Ganz Catheters (K160084) received a 510(k) decision of Substantially Equivalent on May 3, 2016, 109 days after the submission was received.

What is the product code of K160084?

The FDA product code is DYG – Catheter, Flow Directed, a Class II (moderate risk) device regulated under 21 CFR 870.1240.