Cleared Traditional

K872327 - WHIRLPOOL AERATOR WB700, WB800, WB900, WB975 (FDA 510(k) Clearance)

Class II Physical Medicine device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K872327 · Associated Mills, Inc. · Physical Medicine device
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Sep 1987
Decision
79d
Days
Class 2
Risk

K872327 is an FDA 510(k) clearance for the WHIRLPOOL AERATOR WB700, WB800, WB900, WB975. Classified as Bath, Hydro-massage (product code ILJ), Class II - Special Controls.

Submitted by Associated Mills, Inc. (Chicago, US). The FDA issued a Cleared decision on September 4, 1987 after a review of 79 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5100 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Associated Mills, Inc. devices

Submission Details

510(k) Number K872327 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 17, 1987
Decision Date September 04, 1987
Days to Decision 79 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
36d faster than avg
Panel avg: 115d · This submission: 79d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code ILJ Bath, Hydro-massage
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5100
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.