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FDA 510(k)

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

K-Number: K920722 · 1992-04-13

Decision Date1992-04-13
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

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 1992-04-13 under 510(k) number K920722. 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 X-RAY DIAGNOSTIC TABLE YSF-200-30-90?

X-RAY DIAGNOSTIC TABLE YSF-200-30-90 is a medical device that received FDA 510(k) clearance on 1992-04-13. The listed applicant is Shimadzu Medical Systems. The 510(k) number is K920722.

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

X-RAY DIAGNOSTIC TABLE YSF-200-30-90 received FDA 510(k) clearance on 1992-04-13, under 510(k) number K920722.

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

The FDA product code for 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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