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Personal Kinetigraph (PKG)

GKC MANUFACTURING PTY LTD · Model 2000-LOG-004 · UDI-DI 09359011000303

Prescription
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510(k) clearances
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Adverse events
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Recalls
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Facilities

Description

The Personal Kinetigraph (PKG) is intended to quantify kinematics of movement disorder symptoms in conditions such as Parkinson's disease, including tremor, bradykinesia and dyskinesia.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.