Cleared Traditional

K944308 - JAMES LECKEY FREE STANDER

K944308 is an FDA 510(k) clearance for JAMES LECKEY FREE STANDER, manufactured by James Leckey Design. The device is a Class 1 Physical Medicine device with product code INW cleared through the Traditional 510(k) pathway after a 111-day FDA review.

K944308 · James Leckey Design · Physical Medicine device
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Dec 1994
Decision
111d
Days
Class 1
Risk

K944308 is an FDA 510(k) clearance for the JAMES LECKEY FREE STANDER. Classified as Table, Mechanical (product code INW), Class I - General Controls.

Submitted by James Leckey Design (Lawerence, US). The FDA issued a Cleared decision on December 22, 1994 after a review of 111 days - within the typical 510(k) review window.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3750 - 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 James Leckey Design devices

FDA 510(k) Submission Details - K944308

510(k) Number K944308 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 02, 1994
Decision Date December 22, 1994
Days to Decision 111 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
4d faster than avg
Panel avg: 115d · This submission: 111d
Pathway characteristics
Predicate-based equivalence.

INW Device Classification - Class 1, General Controls

Product Code INW Table, Mechanical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3750
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.