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FDA 510(k)

DuoprossTM Smart Cap (Type I)

K-Number: K252518 · 2025-12-17

Decision Date2025-12-17
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DuoprossTM Smart Cap (Type I) is the device name listed in this FDA 510(k) record. The listed applicant is Duopross Meditech Corporate. It received FDA 510(k) clearance on 2025-12-17 under 510(k) 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. The listed applicant is Duopross Meditech Corporate. The 510(k) number is K252518.

When did DuoprossTM Smart Cap (Type I) receive FDA 510(k) clearance?

DuoprossTM Smart Cap (Type I) received FDA 510(k) clearance on 2025-12-17, under 510(k) number K252518.

Who is the listed applicant for DuoprossTM Smart Cap (Type I)?

The FDA 510(k) record lists Duopross Meditech Corporate as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DuoprossTM Smart Cap (Type I)?

The FDA product code for DuoprossTM Smart Cap (Type I) is FMF.

Related Devices (Code: FMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.