FDA 510(k)

JLK-CTP

K-Number: K242556 · 2024-10-16

Decision Date2024-10-16

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

JLK-CTP is the device name listed in this FDA 510(k) record. The listed applicant is JLK, Inc.. It received FDA 510(k) clearance on 2024-10-16 under 510(k) 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. The listed applicant is JLK, Inc.. The 510(k) number is K242556.

When did JLK-CTP receive FDA 510(k) clearance?

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

Who is the listed applicant for JLK-CTP?

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

What is the FDA product code for JLK-CTP?

The FDA product code for JLK-CTP is LLZ.

Other records listing JLK, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252421JLK-NCCT K243611JLK-SDH K250348JLK-AILink K243363JLK-ICH K242709JLK-PWI K241480JBS-LVO

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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.