MAGMA XHF-30, XHF-40, XHF-50
K-Number: K926365 · 1993-03-26
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Device Summary
Frequently Asked Questions
What is the MAGMA XHF-30, XHF-40, XHF-50?
MAGMA XHF-30, XHF-40, XHF-50 is a medical device that received FDA 510(k) clearance on 1993-03-26. The listed applicant is Imaging and X-Ray Intl., Inc.. The 510(k) number is K926365.
When did MAGMA XHF-30, XHF-40, XHF-50 receive FDA 510(k) clearance?
MAGMA XHF-30, XHF-40, XHF-50 received FDA 510(k) clearance on 1993-03-26, under 510(k) number K926365.
Who is the listed applicant for MAGMA XHF-30, XHF-40, XHF-50?
The FDA 510(k) record lists Imaging and X-Ray Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAGMA XHF-30, XHF-40, XHF-50?
The FDA product code for MAGMA XHF-30, XHF-40, XHF-50 is IZO.
Related Clinical Trials
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.
Related Devices (Code: IZO)
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.
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