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FDA 510(k)

LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270

K-Number: K950571 · 1995-03-31

Decision Date1995-03-31
Product CodeIZF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270 is the device name listed in this FDA 510(k) record. The listed applicant is Continental X-Ray Corp.. It received FDA 510(k) clearance on 1995-03-31 under 510(k) number K950571. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270?

LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270 is a medical device that received FDA 510(k) clearance on 1995-03-31. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K950571.

When did LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270 receive FDA 510(k) clearance?

LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270 received FDA 510(k) clearance on 1995-03-31, under 510(k) number K950571.

Who is the listed applicant for LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270?

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 LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270?

The FDA product code for LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270 is IZF.

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.

View all 27 devices →

Related Devices (Code: IZF)

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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