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FDA 510(k)

Invia Ease Negative Pressure Wound Therapy (NPWT) System

K-Number: K214112 · 2022-07-26

ApplicantMedela AG
Decision Date2022-07-26
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Invia Ease Negative Pressure Wound Therapy (NPWT) System is a medical device manufactured by Medela AG. It received FDA 510(k) clearance on 2022-07-26 under approval number K214112. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Invia Ease Negative Pressure Wound Therapy (NPWT) System?

Invia Ease Negative Pressure Wound Therapy (NPWT) System is a medical device that received FDA 510(k) clearance on 2022-07-26. It is manufactured by Medela AG. The 510(k) number is K214112.

When was Invia Ease Negative Pressure Wound Therapy (NPWT) System approved by the FDA?

Invia Ease Negative Pressure Wound Therapy (NPWT) System received FDA 510(k) clearance on 2022-07-26, under approval number K214112.

What company makes Invia Ease Negative Pressure Wound Therapy (NPWT) System?

Invia Ease Negative Pressure Wound Therapy (NPWT) System is manufactured by Medela AG.

What is the FDA product code for Invia Ease Negative Pressure Wound Therapy (NPWT) System?

The FDA product code for Invia Ease Negative Pressure Wound Therapy (NPWT) System is OMP.

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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.