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FDA 510(k)

CODA CX1 MOTION ANALYSIS SYSTEM

K-Number: K033514 · 2004-01-06

ApplicantCharnwood Dynamics , Ltd.
Decision Date2004-01-06
Product CodeLXJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CODA CX1 MOTION ANALYSIS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Charnwood Dynamics , Ltd.. It received FDA 510(k) clearance on 2004-01-06 under 510(k) number K033514. The device is classified under product code LXJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODA CX1 MOTION ANALYSIS SYSTEM?

CODA CX1 MOTION ANALYSIS SYSTEM is a medical device that received FDA 510(k) clearance on 2004-01-06. The listed applicant is Charnwood Dynamics , Ltd.. The 510(k) number is K033514.

When did CODA CX1 MOTION ANALYSIS SYSTEM receive FDA 510(k) clearance?

CODA CX1 MOTION ANALYSIS SYSTEM received FDA 510(k) clearance on 2004-01-06, under 510(k) number K033514.

Who is the listed applicant for CODA CX1 MOTION ANALYSIS SYSTEM?

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

What is the FDA product code for CODA CX1 MOTION ANALYSIS SYSTEM?

The FDA product code for CODA CX1 MOTION ANALYSIS SYSTEM is LXJ.

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Related Devices (Code: LXJ)

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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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