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FDA 510(k)

InterView XP; InterView FUSION

K-Number: K221984 · 2023-03-29

ApplicantMediso Medical Imaging Systems, Lttd.
Decision Date2023-03-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

InterView XP; InterView FUSION is a medical device manufactured by Mediso Medical Imaging Systems, Lttd.. It received FDA 510(k) clearance on 2023-03-29 under approval number K221984. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InterView XP; InterView FUSION?

InterView XP; InterView FUSION is a medical device that received FDA 510(k) clearance on 2023-03-29. It is manufactured by Mediso Medical Imaging Systems, Lttd.. The 510(k) number is K221984.

When was InterView XP; InterView FUSION approved by the FDA?

InterView XP; InterView FUSION received FDA 510(k) clearance on 2023-03-29, under approval number K221984.

What company makes InterView XP; InterView FUSION?

InterView XP; InterView FUSION is manufactured by Mediso Medical Imaging Systems, Lttd..

What is the FDA product code for InterView XP; InterView FUSION?

The FDA product code for InterView XP; InterView FUSION is LLZ.

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Official Source

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