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FDA 510(k)

eMVFit (MVF-10M)

K-Number: K240992 · 2024-10-10

ApplicantWeero Co., Ltd.
Decision Date2024-10-10
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

eMVFit (MVF-10M) is a medical device manufactured by Weero Co., Ltd.. It received FDA 510(k) clearance on 2024-10-10 under approval number K240992. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the eMVFit (MVF-10M)?

eMVFit (MVF-10M) is a medical device that received FDA 510(k) clearance on 2024-10-10. It is manufactured by Weero Co., Ltd.. The 510(k) number is K240992.

When was eMVFit (MVF-10M) approved by the FDA?

eMVFit (MVF-10M) received FDA 510(k) clearance on 2024-10-10, under approval number K240992.

What company makes eMVFit (MVF-10M)?

eMVFit (MVF-10M) is manufactured by Weero Co., Ltd..

What is the FDA product code for eMVFit (MVF-10M)?

The FDA product code for eMVFit (MVF-10M) is IPF.

Other Devices by Weero Co., Ltd.

K240991eMVFit (MVF-10M) K241433EVE Synergy (EVE-20M) K253261Apollo Quattro (APQ-10M)

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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.

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