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FDA 510(k)

SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90

K-Number: K925175 · 1992-11-27

Decision Date1992-11-27
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90 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 1992-11-27 under 510(k) number K925175. The device is classified under product code IXR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90?

SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90 is a medical device that received FDA 510(k) clearance on 1992-11-27. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K925175.

When did SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90 receive FDA 510(k) clearance?

SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90 received FDA 510(k) clearance on 1992-11-27, under 510(k) number K925175.

Who is the listed applicant for SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90?

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 SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90?

The FDA product code for SHIMADZU X-RAY DIAGNOSTIC TABLE YSF-200 30/90 is IXR.

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.

View all 90 devices →

Related Devices (Code: IXR)

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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