Idys® LIF
K-Number: K243670 · 2024-12-31
ApplicantClariance
Decision Date2024-12-31
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Idys® LIF is a medical device manufactured by Clariance. It received FDA 510(k) clearance on 2024-12-31 under approval number K243670. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Idys® LIF?
Idys® LIF is a medical device that received FDA 510(k) clearance on 2024-12-31. It is manufactured by Clariance. The 510(k) number is K243670.
When was Idys® LIF approved by the FDA?
Idys® LIF received FDA 510(k) clearance on 2024-12-31, under approval number K243670.
What company makes Idys® LIF?
Idys® LIF is manufactured by Clariance.
What is the FDA product code for Idys® LIF?
The FDA product code for Idys® LIF is MAX.
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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.