FDA 510(k)

CDMX

K-Number: K010915 · 2001-05-21

Decision Date2001-05-21

Product CodeMUH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

CDMX is the device name listed in this FDA 510(k) record. The listed applicant is Camsight Co., Inc.. It received FDA 510(k) clearance on 2001-05-21 under 510(k) number K010915. 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 CDMX?

CDMX is a medical device that received FDA 510(k) clearance on 2001-05-21. The listed applicant is Camsight Co., Inc.. The 510(k) number is K010915.

When did CDMX receive FDA 510(k) clearance?

CDMX received FDA 510(k) clearance on 2001-05-21, under 510(k) number K010915.

Who is the listed applicant for CDMX?

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

What is the FDA product code for CDMX?

The FDA product code for CDMX is MUH.

Other records listing Camsight Co., Inc. 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.

K063646OPTI K053221CDMX-H

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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.