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FDA 510(k)

MENTAMOVE

K-Number: K040849 · 2004-10-01

ApplicantCole & Associates
Decision Date2004-10-01
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MENTAMOVE is the device name listed in this FDA 510(k) record. The listed applicant is Cole & Associates. It received FDA 510(k) clearance on 2004-10-01 under 510(k) number K040849. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTAMOVE?

MENTAMOVE is a medical device that received FDA 510(k) clearance on 2004-10-01. The listed applicant is Cole & Associates. The 510(k) number is K040849.

When did MENTAMOVE receive FDA 510(k) clearance?

MENTAMOVE received FDA 510(k) clearance on 2004-10-01, under 510(k) number K040849.

Who is the listed applicant for MENTAMOVE?

The FDA 510(k) record lists Cole & Associates as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MENTAMOVE?

The FDA product code for MENTAMOVE is IPF.

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Related Devices (Code: IPF)

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.

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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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