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FDA 510(k)

CDX DIGITAL X-RAY IMAGING SYSTEM

K-Number: K042736 · 2004-10-13

ApplicantCnc Imaging, Inc.
Decision Date2004-10-13
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CDX DIGITAL X-RAY IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cnc Imaging, Inc.. It received FDA 510(k) clearance on 2004-10-13 under 510(k) number K042736. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDX DIGITAL X-RAY IMAGING SYSTEM?

CDX DIGITAL X-RAY IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 2004-10-13. The listed applicant is Cnc Imaging, Inc.. The 510(k) number is K042736.

When did CDX DIGITAL X-RAY IMAGING SYSTEM receive FDA 510(k) clearance?

CDX DIGITAL X-RAY IMAGING SYSTEM received FDA 510(k) clearance on 2004-10-13, under 510(k) number K042736.

Who is the listed applicant for CDX DIGITAL X-RAY IMAGING SYSTEM?

The FDA 510(k) record lists Cnc Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CDX DIGITAL X-RAY IMAGING SYSTEM?

The FDA product code for CDX DIGITAL X-RAY IMAGING SYSTEM is MUH.

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Related Devices (Code: MUH)

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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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