Cleared Traditional

K925036 - HANDY VIBRO BELT

K925036 is an FDA 510(k) clearance for HANDY VIBRO BELT, manufactured by Cosmesearch, Inc.. The device is a Class 1 Physical Medicine device with product code ISA cleared through the Traditional 510(k) pathway after a 267-day FDA review.

K925036 · Cosmesearch, Inc. · Physical Medicine device
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Jun 1993
Decision
267d
Days
Class 1
Risk

K925036 is an FDA 510(k) clearance for the HANDY VIBRO BELT. Classified as Massager, Therapeutic, Electric (product code ISA), Class I - General Controls.

Submitted by Cosmesearch, Inc. (Solana Beach, US). The FDA issued a Cleared decision on June 29, 1993 after a review of 267 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Cosmesearch, Inc. devices

FDA 510(k) Submission Details - K925036

510(k) Number K925036 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 05, 1992
Decision Date June 29, 1993
Days to Decision 267 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
152d slower than avg
Panel avg: 115d · This submission: 267d
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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