FDA 510(k)

CDMX-H

K-Number: K053221 · 2006-01-12

Decision Date2006-01-12

Product CodeMUH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

CDMX-H 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 2006-01-12 under 510(k) number K053221. 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-H?

CDMX-H is a medical device that received FDA 510(k) clearance on 2006-01-12. The listed applicant is Camsight Co., Inc.. The 510(k) number is K053221.

When did CDMX-H receive FDA 510(k) clearance?

CDMX-H received FDA 510(k) clearance on 2006-01-12, under 510(k) number K053221.

Who is the listed applicant for CDMX-H?

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-H?

The FDA product code for CDMX-H 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 K010915CDMX

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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.