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FDA 510(k)

CHUMP

K-Number: K030017 · 2003-05-01

ApplicantColours 'N Motion
Decision Date2003-05-01
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CHUMP is the device name listed in this FDA 510(k) record. The listed applicant is Colours 'N Motion. It received FDA 510(k) clearance on 2003-05-01 under 510(k) number K030017. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHUMP?

CHUMP is a medical device that received FDA 510(k) clearance on 2003-05-01. The listed applicant is Colours 'N Motion. The 510(k) number is K030017.

When did CHUMP receive FDA 510(k) clearance?

CHUMP received FDA 510(k) clearance on 2003-05-01, under 510(k) number K030017.

Who is the listed applicant for CHUMP?

The FDA 510(k) record lists Colours 'N Motion as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHUMP?

The FDA product code for CHUMP is IOR.

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Other records listing Colours 'N Motion as applicant

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Related Devices (Code: IOR)

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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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