MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE
K-Number: K912996 · 1992-02-03
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Device Summary
Frequently Asked Questions
What is the MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE?
MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE is a medical device that received FDA 510(k) clearance on 1992-02-03. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K912996.
When did MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE receive FDA 510(k) clearance?
MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE received FDA 510(k) clearance on 1992-02-03, under 510(k) number K912996.
Who is the listed applicant for MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE?
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 MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE?
The FDA product code for MODIF TOP DRIVE BOARD CXT-90 90/90 DIAG TILT TABLE 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 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: 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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