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FDA 510(k)

JLK-CTP

K-Number: K242556 · 2024-10-16

ApplicantJLK, Inc.
Decision Date2024-10-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JLK-CTP is a medical device manufactured by JLK, Inc.. It received FDA 510(k) clearance on 2024-10-16 under approval number K242556. 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 JLK-CTP?

JLK-CTP is a medical device that received FDA 510(k) clearance on 2024-10-16. It is manufactured by JLK, Inc.. The 510(k) number is K242556.

When was JLK-CTP approved by the FDA?

JLK-CTP received FDA 510(k) clearance on 2024-10-16, under approval number K242556.

What company makes JLK-CTP?

JLK-CTP is manufactured by JLK, Inc..

What is the FDA product code for JLK-CTP?

The FDA product code for JLK-CTP is LLZ.

Other Devices by JLK, Inc.

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Related Devices (Code: LLZ)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.