FDA 510(k)

X-VIEW

K-Number: K024186 · 2004-04-01

Decision Date2004-04-01

Product CodeMUH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

X-VIEW is the device name listed in this FDA 510(k) record. The listed applicant is Sometech Corporation. It received FDA 510(k) clearance on 2004-04-01 under 510(k) number K024186. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-VIEW?

X-VIEW is a medical device that received FDA 510(k) clearance on 2004-04-01. The listed applicant is Sometech Corporation. The 510(k) number is K024186.

When did X-VIEW receive FDA 510(k) clearance?

X-VIEW received FDA 510(k) clearance on 2004-04-01, under 510(k) number K024186.

Who is the listed applicant for X-VIEW?

The FDA 510(k) record lists Sometech Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for X-VIEW?

The FDA product code for X-VIEW is MUH.

Other records listing Sometech Corporation as applicant

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.

K121401TENDER TOUCH K031436MEDISCOPE

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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.