Klockner Kits
K-Number: K243128 · 2024-12-18
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.