InterView XP; InterView FUSION
K-Number: K221984 · 2023-03-29
Device Summary
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. The listed applicant is Mediso Medical Imaging Systems, Lttd.. The 510(k) number is K221984.
When did InterView XP; InterView FUSION receive FDA 510(k) clearance?
InterView XP; InterView FUSION received FDA 510(k) clearance on 2023-03-29, under 510(k) number K221984.
Who is the listed applicant for InterView XP; InterView FUSION?
The FDA 510(k) record lists Mediso Medical Imaging Systems, Lttd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for InterView XP; InterView FUSION?
The FDA product code for InterView XP; InterView FUSION is LLZ.
Related Devices (Code: LLZ)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.