Cleared Traditional

K800068 - ELECTRICAL MUSCLE STIMULATOR (EMS)

K800068 is an FDA 510(k) clearance for ELECTRICAL MUSCLE STIMULATOR (EMS), manufactured by Staodynamics, Inc.. The device is a Class 2 Physical Medicine device with product code IPF cleared through the Traditional 510(k) pathway after a 25-day FDA review.

K800068 · Staodynamics, Inc. · Physical Medicine device
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Feb 1980
Decision
25d
Days
Class 2
Risk

K800068 is an FDA 510(k) clearance for the ELECTRICAL MUSCLE STIMULATOR (EMS). Classified as Stimulator, Muscle, Powered (product code IPF), Class II - Special Controls.

Submitted by Staodynamics, Inc. (Walker, US). The FDA issued a Cleared decision on February 5, 1980 after a review of 25 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5850 - 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 Staodynamics, Inc. devices

FDA 510(k) Submission Details - K800068

510(k) Number K800068 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 11, 1980
Decision Date February 05, 1980
Days to Decision 25 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
90d faster than avg
Panel avg: 115d · This submission: 25d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IPF Device Classification - Class 2, Special Controls

Product Code IPF Stimulator, Muscle, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 890.5850
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 - IPF Stimulator, Muscle, Powered

All 275
Devices cleared under the same product code (IPF) and FDA review panel - the closest regulatory comparables to K800068.
ZIMMER ELECTRICAL MUSCLE STIMULATOR
K803064 · Zimmer, Inc. · Dec 1980
INTELECT
K801790 · Chattanooga Group, Inc. · Aug 1980
MOD. 3127 NEUROMUSCULAR STIMULATOR
K800484 · Medtronic Vascular · May 1980
HVG-100
K790033 · Elmed, Inc. · Feb 1979
MUSCLE STIMULATOR, ELECTRICAL
K781113 · Rich-Mar Corp. · Sep 1978
STEMPLEX
K781167 · Rich-Mar Corp. · Sep 1978