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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 a medical device manufactured by Ilooda Co,., Ltd.. It received FDA 510(k) clearance on 2024-11-21 under approval 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. It is manufactured by Ilooda Co,., Ltd.. The 510(k) number is K241157.

When was Secret MAX Multi-platform RF System approved by the FDA?

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

What company makes Secret MAX Multi-platform RF System?

Secret MAX Multi-platform RF System is manufactured by Ilooda Co,., Ltd..

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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Related PubMed Literature

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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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