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FDA 510(k)

WiEMSpro

K-Number: K211298 · 2022-08-25

ApplicantMedical Cables S.L.
Decision Date2022-08-25
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WiEMSpro is a medical device manufactured by Medical Cables S.L.. It received FDA 510(k) clearance on 2022-08-25 under approval number K211298. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WiEMSpro?

WiEMSpro is a medical device that received FDA 510(k) clearance on 2022-08-25. It is manufactured by Medical Cables S.L.. The 510(k) number is K211298.

When was WiEMSpro approved by the FDA?

WiEMSpro received FDA 510(k) clearance on 2022-08-25, under approval number K211298.

What company makes WiEMSpro?

WiEMSpro is manufactured by Medical Cables S.L..

What is the FDA product code for WiEMSpro?

The FDA product code for WiEMSpro is NGX.

Other Devices by Medical Cables S.L.

K181955WiEMSpro

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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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