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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is El.En S.P.A.. It received FDA 510(k) clearance on 2023-12-19 under 510(k) 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. The listed applicant is El.En S.P.A.. The 510(k) number is K233470.

When did DEKA LILY receive FDA 510(k) clearance?

DEKA LILY received FDA 510(k) clearance on 2023-12-19, under 510(k) number K233470.

Who is the listed applicant for DEKA LILY?

The FDA 510(k) record lists El.En S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEKA LILY?

The FDA product code for DEKA LILY is NGX.

Other records listing El.En S.P.A. as applicant

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Related Devices (Code: 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.

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