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FDA 510(k)

RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004

K-Number: K911267 · 1991-04-03

ApplicantTri W-G, Inc.
Decision Date1991-04-03
Product CodeIXR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004 is the device name listed in this FDA 510(k) record. The listed applicant is Tri W-G, Inc.. It received FDA 510(k) clearance on 1991-04-03 under 510(k) number K911267. 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 RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004?

RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004 is a medical device that received FDA 510(k) clearance on 1991-04-03. The listed applicant is Tri W-G, Inc.. The 510(k) number is K911267.

When did RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004 receive FDA 510(k) clearance?

RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004 received FDA 510(k) clearance on 1991-04-03, under 510(k) number K911267.

Who is the listed applicant for RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004?

The FDA 510(k) record lists Tri W-G, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004?

The FDA product code for RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004 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 Tri W-G, Inc. 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 35 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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