RADIOGRAPHIC/FLUOROSCOPIC TABLE MODEL 9004
K-Number: K911267 · 1991-04-03
Advertisement
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement