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FDA 510(k)

Klockner Kits

K-Number: K243128 · 2024-12-18

ApplicantSOADCO, S.L.
Decision Date2024-12-18
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Klockner Kits is the device name listed in this FDA 510(k) record. The listed applicant is SOADCO, S.L.. It received FDA 510(k) clearance on 2024-12-18 under 510(k) number K243128. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Klockner Kits?

Klockner Kits is a medical device that received FDA 510(k) clearance on 2024-12-18. The listed applicant is SOADCO, S.L.. The 510(k) number is K243128.

When did Klockner Kits receive FDA 510(k) clearance?

Klockner Kits received FDA 510(k) clearance on 2024-12-18, under 510(k) number K243128.

Who is the listed applicant for Klockner Kits?

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

What is the FDA product code for Klockner Kits?

The FDA product code for Klockner Kits is KCT.

Other records listing SOADCO, S.L. 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.

Related Devices (Code: KCT)

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.

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.