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FDA 510(k)

SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM

K-Number: K925107 · 1993-01-15

Decision Date1993-01-15
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Shimadzu Medical Systems. It received FDA 510(k) clearance on 1993-01-15 under 510(k) number K925107. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM?

SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K925107.

When did SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM receive FDA 510(k) clearance?

SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM received FDA 510(k) clearance on 1993-01-15, under 510(k) number K925107.

Who is the listed applicant for SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM?

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

What is the FDA product code for SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM?

The FDA product code for SMT-50XM MAGNETIC RESONANCE IMAGING SYSTEM is LNH.

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.

Other records listing Shimadzu Medical Systems 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.

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Related Devices (Code: LNH)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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