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FDA 510(k)

CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET

K-Number: K072960 · 2007-11-08

ApplicantCdp, Ltd.
Decision Date2007-11-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET is the device name listed in this FDA 510(k) record. The listed applicant is Cdp, Ltd.. It received FDA 510(k) clearance on 2007-11-08 under 510(k) number K072960. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET?

CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET is a medical device that received FDA 510(k) clearance on 2007-11-08. The listed applicant is Cdp, Ltd.. The 510(k) number is K072960.

When did CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET receive FDA 510(k) clearance?

CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET received FDA 510(k) clearance on 2007-11-08, under 510(k) number K072960.

Who is the listed applicant for CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET?

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

What is the FDA product code for CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET?

The FDA product code for CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET is LLZ.

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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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