Cleared Traditional

K950322 - RELAXY-THE WONDER HAND

K950322 is an FDA 510(k) clearance for RELAXY-THE WONDER HAND, manufactured by Kinsei Shiatsu, Inc.. The device is a Class 1 Physical Medicine device with product code ISA cleared through the Traditional 510(k) pathway after a 19-day FDA review.

K950322 · Kinsei Shiatsu, Inc. · Physical Medicine device
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Feb 1995
Decision
19d
Days
Class 1
Risk

K950322 is an FDA 510(k) clearance for the RELAXY-THE WONDER HAND. Classified as Massager, Therapeutic, Electric (product code ISA), Class I - General Controls.

Submitted by Kinsei Shiatsu, Inc. (Torrance, US). The FDA issued a Cleared decision on February 14, 1995 after a review of 19 days - a notably fast clearance cycle.

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: 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 Kinsei Shiatsu, Inc. devices

FDA 510(k) Submission Details - K950322

510(k) Number K950322 FDA.gov
FDA Decision Cleared Substantially Equivalent - NSE Converted (SN)
Date Received January 26, 1995
Decision Date February 14, 1995
Days to Decision 19 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
96d faster than avg
Panel avg: 115d · This submission: 19d
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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