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FDA 510(k)

CES ULTRA

K-Number: K062284 · 2007-04-05

ApplicantNeuro-Fitness, LLC
Decision Date2007-04-05
Product CodeQJQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CES ULTRA is the device name listed in this FDA 510(k) record. The listed applicant is Neuro-Fitness, LLC. It received FDA 510(k) clearance on 2007-04-05 under 510(k) number K062284. The device is classified under product code QJQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CES ULTRA?

CES ULTRA is a medical device that received FDA 510(k) clearance on 2007-04-05. The listed applicant is Neuro-Fitness, LLC. The 510(k) number is K062284.

When did CES ULTRA receive FDA 510(k) clearance?

CES ULTRA received FDA 510(k) clearance on 2007-04-05, under 510(k) number K062284.

Who is the listed applicant for CES ULTRA?

The FDA 510(k) record lists Neuro-Fitness, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CES ULTRA?

The FDA product code for CES ULTRA is QJQ.

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Related Devices (Code: QJQ)

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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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