Cleared Traditional

K901796 - PODOFLEX EXERCISER-PASSIVE-FOOT/ANKLE

K901796 is the FDA 510(k) clearance for PODOFLEX EXERCISER-PASSIVE-FOOT/ANKLE by Component Equipment Mfg., Inc.. It is a Class 1 Physical Medicine device (product code ISA) cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K901796 · Component Equipment Mfg., Inc. · Physical Medicine device
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Jun 1990
Decision
48d
Days
Class 1
Risk

K901796 is an FDA 510(k) clearance for the PODOFLEX EXERCISER-PASSIVE-FOOT/ANKLE. Classified as Massager, Therapeutic, Electric (product code ISA), Class I - General Controls.

Submitted by Component Equipment Mfg., Inc. (Colorado Springs, US). The FDA issued a Cleared decision on June 6, 1990 after a review of 48 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 Component Equipment Mfg., Inc. devices

Submission Details

510(k) Number K901796 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 19, 1990
Decision Date June 06, 1990
Days to Decision 48 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
67d faster than avg
Panel avg: 115d · This submission: 48d
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 15
Devices cleared under the same product code (ISA) and FDA review panel - the closest regulatory comparables to K901796.
OMRON MASSAGER MODEL HM-45
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OMRON MASSAGER MODEL HM-102
K935581 · Omron Healthcare, Inc. · Mar 1994
SENSORY ROLLER MASSAGER
K833090 · Maddak, Inc. · Oct 1983
MAGIC CUSHION MASSAGER
K810447 · Fred Sammons, Inc. · Mar 1981