Tubing Pack
K-Number: K171979 · 2017-10-27
ApplicantMedtronic, Inc.
Decision Date2017-10-27
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Tubing Pack is a medical device manufactured by Medtronic, Inc.. It received FDA 510(k) clearance on 2017-10-27 under approval number K171979. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Tubing Pack?
Tubing Pack is a medical device that received FDA 510(k) clearance on 2017-10-27. It is manufactured by Medtronic, Inc.. The 510(k) number is K171979.
When was Tubing Pack approved by the FDA?
Tubing Pack received FDA 510(k) clearance on 2017-10-27, under approval number K171979.
What company makes Tubing Pack?
Tubing Pack is manufactured by Medtronic, Inc..
What is the FDA product code for Tubing Pack?
The FDA product code for Tubing Pack is DWF.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.