KBA3D
K-Number: K223841 · 2023-05-30
ApplicantS.M.A.I.O
Decision Date2023-05-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
KBA3D is a medical device manufactured by S.M.A.I.O. It received FDA 510(k) clearance on 2023-05-30 under approval number K223841. 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 KBA3D?
KBA3D is a medical device that received FDA 510(k) clearance on 2023-05-30. It is manufactured by S.M.A.I.O. The 510(k) number is K223841.
When was KBA3D approved by the FDA?
KBA3D received FDA 510(k) clearance on 2023-05-30, under approval number K223841.
What company makes KBA3D?
KBA3D is manufactured by S.M.A.I.O.
What is the FDA product code for KBA3D?
The FDA product code for KBA3D is LLZ.
Other Devices by S.M.A.I.O
Related Devices (Code: LLZ)
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.