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FDA 510(k)

Secret MAX Multi-platform RF System

K-Number: K241157 · 2024-11-21

ApplicantIlooda Co,., Ltd.
Decision Date2024-11-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Secret MAX Multi-platform RF System 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 2024-11-21 under 510(k) number K241157. 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 MAX Multi-platform RF System?

Secret MAX Multi-platform RF System is a medical device that received FDA 510(k) clearance on 2024-11-21. The listed applicant is Ilooda Co,., Ltd.. The 510(k) number is K241157.

When did Secret MAX Multi-platform RF System receive FDA 510(k) clearance?

Secret MAX Multi-platform RF System received FDA 510(k) clearance on 2024-11-21, under 510(k) number K241157.

Who is the listed applicant for Secret MAX Multi-platform RF System?

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 MAX Multi-platform RF System?

The FDA product code for Secret MAX Multi-platform RF System 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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