Multi M Series
K-Number: K250826 · 2025-06-12
ApplicantDmax Co., Ltd.
Decision Date2025-06-12
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Multi M Series is a medical device manufactured by Dmax Co., Ltd.. It received FDA 510(k) clearance on 2025-06-12 under approval number K250826. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Multi M Series?
Multi M Series is a medical device that received FDA 510(k) clearance on 2025-06-12. It is manufactured by Dmax Co., Ltd.. The 510(k) number is K250826.
When was Multi M Series approved by the FDA?
Multi M Series received FDA 510(k) clearance on 2025-06-12, under approval number K250826.
What company makes Multi M Series?
Multi M Series is manufactured by Dmax Co., Ltd..
What is the FDA product code for Multi M Series?
The FDA product code for Multi M Series is EIH.
Related Clinical Trials
Other Devices by Dmax Co., Ltd.
Related Devices (Code: EIH)
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.