DuoprossTM Smart Cap (Type I)
K-Number: K252518 · 2025-12-17
ApplicantDuopross Meditech Corporate
Decision Date2025-12-17
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
DuoprossTM Smart Cap (Type I) is a medical device manufactured by Duopross Meditech Corporate. It received FDA 510(k) clearance on 2025-12-17 under approval number K252518. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DuoprossTM Smart Cap (Type I)?
DuoprossTM Smart Cap (Type I) is a medical device that received FDA 510(k) clearance on 2025-12-17. It is manufactured by Duopross Meditech Corporate. The 510(k) number is K252518.
When was DuoprossTM Smart Cap (Type I) approved by the FDA?
DuoprossTM Smart Cap (Type I) received FDA 510(k) clearance on 2025-12-17, under approval number K252518.
What company makes DuoprossTM Smart Cap (Type I)?
DuoprossTM Smart Cap (Type I) is manufactured by Duopross Meditech Corporate.
What is the FDA product code for DuoprossTM Smart Cap (Type I)?
The FDA product code for DuoprossTM Smart Cap (Type I) is FMF.
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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.