Cleared Traditional

OMRON MASSAGER MODEL HM-45 (K935459) - FDA 510(k) Clearance

Class I Physical Medicine device.

Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1994
Decision
112d
Days
Class 1
Risk

K935459 is an FDA 510(k) clearance for the OMRON MASSAGER MODEL HM-45. Classified as Massager, Therapeutic, Electric (product code ISA), Class I - General Controls.

Submitted by Omron Healthcare, Inc. (Vernon Hills, US). The FDA issued a Cleared decision on March 4, 1994 after a review of 112 days - within the typical 510(k) review window.

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 Omron Healthcare, Inc. devices

Submission Details

510(k) Number K935459 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 12, 1993
Decision Date March 04, 1994
Days to Decision 112 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
3d faster than avg
Panel avg: 115d · This submission: 112d
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 99
Devices cleared under the same product code (ISA) and FDA review panel - the closest regulatory comparables to K935459.
VMAT PRO
K243488 · Termosalud · Feb 2025
ShockPhysio Mobile (model SW3200 Basic)
K240358 · Shenzhen Dongdixin Technology Co., Ltd. · Jun 2024
BTL-094
K221865 · BTL Industries, Inc. · Apr 2023
Omnispec ED1000
K210166 · Medispec, Ltd. · Jan 2023
OW100S (model OW100S-US)
K213120 · Tissue Regeneration Technologies, LLC Dba AS Softwave Trt · Oct 2022
DolorClast Radial
K220538 · E.M.S Electro Medical Systems S.A · Jul 2022