CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111
K-Number: K912516 · 1991-11-19
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Device Summary
Frequently Asked Questions
What is the CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111?
CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111 is a medical device that received FDA 510(k) clearance on 1991-11-19. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K912516.
When did CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111 receive FDA 510(k) clearance?
CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111 received FDA 510(k) clearance on 1991-11-19, under 510(k) number K912516.
Who is the listed applicant for CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111?
The FDA 510(k) record lists Continental X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111?
The FDA product code for CLASSIC-II 4-WAY HORIZONTAL TABLE CAT.# T-9111 is IZZ.
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 Continental X-Ray 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: IZZ)
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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