Cleared Traditional

K924237 - WINDMERE PRELUDE III

K924237 is an FDA 510(k) clearance for WINDMERE PRELUDE III, manufactured by Windmere Corp.. The device is a Class 1 Physical Medicine device with product code ISA cleared through the Traditional 510(k) pathway after a 420-day FDA review.

K924237 · Windmere Corp. · Physical Medicine device
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Oct 1993
Decision
420d
Days
Class 1
Risk

K924237 is an FDA 510(k) clearance for the WINDMERE PRELUDE III. Classified as Massager, Therapeutic, Electric (product code ISA), Class I - General Controls.

Submitted by Windmere Corp. (Miami Lakes, US). The FDA issued a Cleared decision on October 18, 1993 after a review of 420 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5660 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Physical Medicine submissions.

View all Windmere Corp. devices

FDA 510(k) Submission Details - K924237

510(k) Number K924237 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 24, 1992
Decision Date October 18, 1993
Days to Decision 420 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
305d slower than avg
Panel avg: 115d · This submission: 420d
Pathway characteristics
Predicate-based equivalence.

ISA Device Classification - Class 1, General Controls

Product Code ISA Massager, Therapeutic, Electric
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5660
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.

Regulatory Peers - ISA Massager, Therapeutic, Electric

All 26
Devices cleared under the same product code (ISA) and FDA review panel - the closest regulatory comparables to K924237.
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