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FDA 510(k)

Secret Pro

K-Number: K233374 · 2023-12-14

ApplicantIlooda Co,., Ltd.
Decision Date2023-12-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Secret Pro is the device name listed in this FDA 510(k) record. The listed applicant is Ilooda Co,., Ltd.. It received FDA 510(k) clearance on 2023-12-14 under 510(k) number K233374. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Secret Pro?

Secret Pro is a medical device that received FDA 510(k) clearance on 2023-12-14. The listed applicant is Ilooda Co,., Ltd.. The 510(k) number is K233374.

When did Secret Pro receive FDA 510(k) clearance?

Secret Pro received FDA 510(k) clearance on 2023-12-14, under 510(k) number K233374.

Who is the listed applicant for Secret Pro?

The FDA 510(k) record lists Ilooda Co,., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Secret Pro?

The FDA product code for Secret Pro is GEI.

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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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