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FDA 510(k)

INTEGRATED MOVEMENT ANALYZER

K-Number: K944787 · 1995-07-07

ApplicantMaryrose
Decision Date1995-07-07
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTEGRATED MOVEMENT ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Maryrose. It received FDA 510(k) clearance on 1995-07-07 under 510(k) number K944787. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEGRATED MOVEMENT ANALYZER?

INTEGRATED MOVEMENT ANALYZER is a medical device that received FDA 510(k) clearance on 1995-07-07. The listed applicant is Maryrose. The 510(k) number is K944787.

When did INTEGRATED MOVEMENT ANALYZER receive FDA 510(k) clearance?

INTEGRATED MOVEMENT ANALYZER received FDA 510(k) clearance on 1995-07-07, under 510(k) number K944787.

Who is the listed applicant for INTEGRATED MOVEMENT ANALYZER?

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

What is the FDA product code for INTEGRATED MOVEMENT ANALYZER?

The FDA product code for INTEGRATED MOVEMENT ANALYZER is IKN.

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Related Devices (Code: IKN)

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.

K172743Natus VikingQuestNatus Neurology IncorporatedK163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.K123902PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)Oktx, LLCK123399MYOVISION 3.0 WIREFREE SYSTEMPrecision Biometrics, Inc.K113074CMAP PROMedical Technologies, Inc.

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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