Drakon and Sequre® Microcatheters
K-Number: K231293 · 2023-06-01
ApplicantAccurate Medical Therapeutics
Decision Date2023-06-01
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Drakon and Sequre® Microcatheters is a medical device manufactured by Accurate Medical Therapeutics. It received FDA 510(k) clearance on 2023-06-01 under approval number K231293. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Drakon and Sequre® Microcatheters?
Drakon and Sequre® Microcatheters is a medical device that received FDA 510(k) clearance on 2023-06-01. It is manufactured by Accurate Medical Therapeutics. The 510(k) number is K231293.
When was Drakon and Sequre® Microcatheters approved by the FDA?
Drakon and Sequre® Microcatheters received FDA 510(k) clearance on 2023-06-01, under approval number K231293.
What company makes Drakon and Sequre® Microcatheters?
Drakon and Sequre® Microcatheters is manufactured by Accurate Medical Therapeutics.
What is the FDA product code for Drakon and Sequre® Microcatheters?
The FDA product code for Drakon and Sequre® Microcatheters is DQO.
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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.