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FDA 510(k)

QuickRad

K-Number: K242838 · 2025-02-21

ApplicantAikenist Technologies Pvt, Ltd.
Decision Date2025-02-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

QuickRad is a medical device manufactured by Aikenist Technologies Pvt, Ltd.. It received FDA 510(k) clearance on 2025-02-21 under approval number K242838. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QuickRad?

QuickRad is a medical device that received FDA 510(k) clearance on 2025-02-21. It is manufactured by Aikenist Technologies Pvt, Ltd.. The 510(k) number is K242838.

When was QuickRad approved by the FDA?

QuickRad received FDA 510(k) clearance on 2025-02-21, under approval number K242838.

What company makes QuickRad?

QuickRad is manufactured by Aikenist Technologies Pvt, Ltd..

What is the FDA product code for QuickRad?

The FDA product code for QuickRad is LLZ.

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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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