Cleared Traditional

K925907 - AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER

K925907 is an FDA 510(k) clearance for AQUASSAGER WM110/W210 & WM120 BODY BASI..., manufactured by Pollenex Corp.. The device is a Class 1 Physical Medicine device with product code ISA cleared through the Traditional 510(k) pathway after a 495-day FDA review.

K925907 · Pollenex Corp. · Physical Medicine device
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Mar 1994
Decision
495d
Days
Class 1
Risk

K925907 is an FDA 510(k) clearance for the AQUASSAGER WM110/W210 & WM120 BODY BASICS MASSAGER. Classified as Massager, Therapeutic, Electric (product code ISA), Class I - General Controls.

Submitted by Pollenex Corp. (Chicago, US). The FDA issued a Cleared decision on March 30, 1994 after a review of 495 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 Pollenex Corp. devices

FDA 510(k) Submission Details - K925907

510(k) Number K925907 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 20, 1992
Decision Date March 30, 1994
Days to Decision 495 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
380d slower than avg
Panel avg: 115d · This submission: 495d
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 28
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