Decision Date2018-06-29
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
TubeClear System is a medical device manufactured by Actuated Medical, Inc.. It received FDA 510(k) clearance on 2018-06-29 under approval number K172556. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the TubeClear System?
TubeClear System is a medical device that received FDA 510(k) clearance on 2018-06-29. It is manufactured by Actuated Medical, Inc.. The 510(k) number is K172556.
When was TubeClear System approved by the FDA?
TubeClear System received FDA 510(k) clearance on 2018-06-29, under approval number K172556.
What company makes TubeClear System?
TubeClear System is manufactured by Actuated Medical, Inc..
What is the FDA product code for TubeClear System?
The FDA product code for TubeClear System is KNT.
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K152246Aquarius Stoma Measuring DeviceDegania Silicone , Ltd.
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Official Source
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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.