Cleared Abbreviated

K032955 - AUTOMOVE

K032955 is an FDA 510(k) clearance for AUTOMOVE, manufactured by Danmeter A/S. The device is a Class 2 Physical Medicine device with product code IPF cleared through the Abbreviated 510(k) pathway after a 84-day FDA review.

K032955 · Danmeter A/S · Physical Medicine device
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Dec 2003
Decision
84d
Days
Class 2
Risk

K032955 is an FDA 510(k) clearance for the AUTOMOVE, MODEL AM800. Classified as Stimulator, Muscle, Powered (product code IPF), Class II - Special Controls.

Submitted by Danmeter A/S (Odense C, DK). The FDA issued a Cleared decision on December 15, 2003 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5850 - the FDA physical medicine device framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Danmeter A/S devices

FDA 510(k) Submission Details - K032955

510(k) Number K032955 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 2003
Decision Date December 15, 2003
Days to Decision 84 days
Submission Type Abbreviated
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
31d faster than avg
Panel avg: 115d · This submission: 84d
Pathway characteristics
Standards-based clearance path.

IPF Device Classification - Class 2, Special Controls

Product Code IPF Stimulator, Muscle, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5850
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Physical Medicine devices follow this clearance model.

Regulatory Peers - IPF Stimulator, Muscle, Powered

All 157
Devices cleared under the same product code (IPF) and FDA review panel - the closest regulatory comparables to K032955.
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