Cleared Traditional

K926339 - BODY RELAXER

K926339 is the FDA 510(k) clearance for BODY RELAXER by Conair Corp.. It is a Class 1 Physical Medicine device (product code ISA) cleared through the Traditional 510(k) pathway after a 444-day FDA review.

K926339 · Conair Corp. · Physical Medicine device
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Mar 1994
Decision
444d
Days
Class 1
Risk

K926339 is an FDA 510(k) clearance for the BODY RELAXER. Classified as Massager, Therapeutic, Electric (product code ISA), Class I - General Controls.

Submitted by Conair Corp. (Stamford, US). The FDA issued a Cleared decision on March 4, 1994 after a review of 444 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 Conair Corp. devices

Submission Details

510(k) Number K926339 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 15, 1992
Decision Date March 04, 1994
Days to Decision 444 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
329d slower than avg
Panel avg: 115d · This submission: 444d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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 24
Devices cleared under the same product code (ISA) and FDA review panel - the closest regulatory comparables to K926339.
BODY FLEX
K942950 · Conair Corp. · Jul 1994
BODY SYSTEM
K942223 · Conair Corp. · Jun 1994
BODY RECHARGER
K940369 · Conair Corp. · Apr 1994
OMRON MASSAGER MODEL HM-45
K935459 · Omron Healthcare, Inc. · Mar 1994
OMBRON TWIN-HEAD MASSAGER MODEL HM-101
K935462 · Omron Healthcare, Inc. · Mar 1994
OMRON MASSAGER MODEL HM-102
K935581 · Omron Healthcare, Inc. · Mar 1994