CEILING MOUNTED TILTING TABLE TANGENT III
K-Number: K880529 · 1988-03-03
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Device Summary
Frequently Asked Questions
What is the CEILING MOUNTED TILTING TABLE TANGENT III?
CEILING MOUNTED TILTING TABLE TANGENT III is a medical device that received FDA 510(k) clearance on 1988-03-03. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K880529.
When did CEILING MOUNTED TILTING TABLE TANGENT III receive FDA 510(k) clearance?
CEILING MOUNTED TILTING TABLE TANGENT III received FDA 510(k) clearance on 1988-03-03, under 510(k) number K880529.
Who is the listed applicant for CEILING MOUNTED TILTING TABLE TANGENT III?
The FDA 510(k) record lists Fischer Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CEILING MOUNTED TILTING TABLE TANGENT III?
The FDA product code for CEILING MOUNTED TILTING TABLE TANGENT III 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 Fischer Imaging Corp. 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.
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