Cleared Traditional

K880699 - ENDOMED CV405

K880699 is an FDA 510(k) clearance for ENDOMED CV405, manufactured by Henley Intl.. The device is a Class 2 Physical Medicine device with product code IPF cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K880699 · Henley Intl. · Physical Medicine device
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May 1988
Decision
70d
Days
Class 2
Risk

K880699 is an FDA 510(k) clearance for the ENDOMED CV405. Classified as Stimulator, Muscle, Powered (product code IPF), Class II - Special Controls.

Submitted by Henley Intl. (Houston, US). The FDA issued a Cleared decision on May 2, 1988 after a review of 70 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.

FDA 510(k) Submission Details - K880699

510(k) Number K880699 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 22, 1988
Decision Date May 02, 1988
Days to Decision 70 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 116d · This submission: 70d
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 547
Devices cleared under the same product code (IPF) and FDA review panel - the closest regulatory comparables to K880699.
MUSCLE STIM. DEVICES, BM 2000,4000,6000,8000
K874232 · Health Systems Intl., Inc. · Mar 1989
SOKEN PLUS(TM) ELECTRONIC MUSCLE STIMULATOR
K881470 · Rehab Medical Specialties, Inc. · Mar 1989
VERIMED MYO/PREMS
K874212 · Verimed Holdings, Inc. · Aug 1988
RICH-MAR G1000 EMS
K880948 · Rich-Mar Corp. · Apr 1988
INTELECT MODEL 120
K880235 · Chattanooga Group, Inc. · Apr 1988
ARCHGAUGE(TM)
K881024 · Archxerciser Corp. · Apr 1988
K880699 · ENDOMED CV405
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