Cleared Traditional

K042650 - BIOMOVE 3000

K042650 is an FDA 510(k) clearance for BIOMOVE 3000, manufactured by Curatronic, Ltd.. The device is a Class 2 Physical Medicine device with product code IPF cleared through the Traditional 510(k) pathway after a 121-day FDA review.

K042650 · Curatronic, Ltd. · Physical Medicine device
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Jan 2005
Decision
121d
Days
Class 2
Risk

K042650 is an FDA 510(k) clearance for the BIOMOVE 3000. Classified as Stimulator, Muscle, Powered (product code IPF), Class II - Special Controls.

Submitted by Curatronic, Ltd. (Heshmonayim, IL). The FDA issued a Cleared decision on January 27, 2005 after a review of 121 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5850 - the FDA physical medicine device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Curatronic, Ltd. devices

FDA 510(k) Submission Details - K042650

510(k) Number K042650 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 28, 2004
Decision Date January 27, 2005
Days to Decision 121 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
6d slower than avg
Panel avg: 115d · This submission: 121d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 204
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