Cleared Traditional

K030437 - RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM

K030437 is an FDA 510(k) clearance for RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM, manufactured by Salton, Inc.. The device is a Class 2 Physical Medicine device with product code IRP cleared through the Traditional 510(k) pathway after a 59-day FDA review.

K030437 · Salton, Inc. · Physical Medicine device
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Apr 2003
Decision
59d
Days
Class 2
Risk

K030437 is an FDA 510(k) clearance for the RELAXOR PERFECT TOUCH AIR MASSAGING SYSTEM. Classified as Massager, Powered Inflatable Tube (product code IRP), Class II - Special Controls.

Submitted by Salton, Inc. (Washington, US). The FDA issued a Cleared decision on April 10, 2003 after a review of 59 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5650 - 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 Salton, Inc. devices

FDA 510(k) Submission Details - K030437

510(k) Number K030437 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 10, 2003
Decision Date April 10, 2003
Days to Decision 59 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
56d faster than avg
Panel avg: 115d · This submission: 59d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IRP Device Classification - Class 2, Special Controls

Product Code IRP Massager, Powered Inflatable Tube
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5650
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.

Regulatory Peers - IRP Massager, Powered Inflatable Tube

All 126
Devices cleared under the same product code (IRP) and FDA review panel - the closest regulatory comparables to K030437.
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ATLANT'S
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