Drivewire 24 Guidewire
K-Number: K233791 · 2024-07-11
ApplicantRapid-Medical , Ltd.
Decision Date2024-07-11
Product CodeMOF
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Drivewire 24 Guidewire is a medical device manufactured by Rapid-Medical , Ltd.. It received FDA 510(k) clearance on 2024-07-11 under approval number K233791. The device is classified under product code MOF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Drivewire 24 Guidewire?
Drivewire 24 Guidewire is a medical device that received FDA 510(k) clearance on 2024-07-11. It is manufactured by Rapid-Medical , Ltd.. The 510(k) number is K233791.
When was Drivewire 24 Guidewire approved by the FDA?
Drivewire 24 Guidewire received FDA 510(k) clearance on 2024-07-11, under approval number K233791.
What company makes Drivewire 24 Guidewire?
Drivewire 24 Guidewire is manufactured by Rapid-Medical , Ltd..
What is the FDA product code for Drivewire 24 Guidewire?
The FDA product code for Drivewire 24 Guidewire is MOF.
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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.