FDA 510(k)

DCM 2.0

K-Number: K020971 · 2002-06-06

Decision Date2002-06-06

Product CodeMUJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DCM 2.0 is the device name listed in this FDA 510(k) record. The listed applicant is Mds Nordion AB. It received FDA 510(k) clearance on 2002-06-06 under 510(k) number K020971. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DCM 2.0?

DCM 2.0 is a medical device that received FDA 510(k) clearance on 2002-06-06. The listed applicant is Mds Nordion AB. The 510(k) number is K020971.

When did DCM 2.0 receive FDA 510(k) clearance?

DCM 2.0 received FDA 510(k) clearance on 2002-06-06, under 510(k) number K020971.

Who is the listed applicant for DCM 2.0?

The FDA 510(k) record lists Mds Nordion AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DCM 2.0?

The FDA product code for DCM 2.0 is MUJ.

Related Devices (Code: MUJ)

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.

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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.