Elos Accurate® Hybrid Base
K-Number: K242025 · 2024-12-10
ApplicantElos Medtech Pinol A/S
Decision Date2024-12-10
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Elos Accurate® Hybrid Base is a medical device manufactured by Elos Medtech Pinol A/S. It received FDA 510(k) clearance on 2024-12-10 under approval number K242025. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Elos Accurate® Hybrid Base?
Elos Accurate® Hybrid Base is a medical device that received FDA 510(k) clearance on 2024-12-10. It is manufactured by Elos Medtech Pinol A/S. The 510(k) number is K242025.
When was Elos Accurate® Hybrid Base approved by the FDA?
Elos Accurate® Hybrid Base received FDA 510(k) clearance on 2024-12-10, under approval number K242025.
What company makes Elos Accurate® Hybrid Base?
Elos Accurate® Hybrid Base is manufactured by Elos Medtech Pinol A/S.
What is the FDA product code for Elos Accurate® Hybrid Base?
The FDA product code for Elos Accurate® Hybrid Base is NHA.
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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.