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 a medical device manufactured by SOADCO, S.L.. It received FDA 510(k) clearance on 2024-12-18 under approval 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. It is manufactured by SOADCO, S.L.. The 510(k) number is K243128.
When was Klockner Kits approved by the FDA?
Klockner Kits received FDA 510(k) clearance on 2024-12-18, under approval number K243128.
What company makes Klockner Kits?
Klockner Kits is manufactured by SOADCO, S.L..
What is the FDA product code for Klockner Kits?
The FDA product code for Klockner Kits is KCT.
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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.