DEKA LILY
K-Number: K233470 · 2023-12-19
ApplicantEl.En S.P.A.
Decision Date2023-12-19
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
DEKA LILY is a medical device manufactured by El.En S.P.A.. It received FDA 510(k) clearance on 2023-12-19 under approval number K233470. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DEKA LILY?
DEKA LILY is a medical device that received FDA 510(k) clearance on 2023-12-19. It is manufactured by El.En S.P.A.. The 510(k) number is K233470.
When was DEKA LILY approved by the FDA?
DEKA LILY received FDA 510(k) clearance on 2023-12-19, under approval number K233470.
What company makes DEKA LILY?
DEKA LILY is manufactured by El.En S.P.A..
What is the FDA product code for DEKA LILY?
The FDA product code for DEKA LILY is NGX.
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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.