Cleared Traditional

K890500 - ELT OR ERGONOMIC LIFT TRAINER

K890500 is an FDA 510(k) clearance for ELT OR ERGONOMIC LIFT TRAINER, manufactured by Physical Health Devices, Inc.. The device is a Class 2 Neurology device with product code HCC cleared through the Traditional 510(k) pathway after a 336-day FDA review.

K890500 · Physical Health Devices, Inc. · Neurology device
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Jan 1990
Decision
336d
Days
Class 2
Risk

K890500 is an FDA 510(k) clearance for the ELT OR ERGONOMIC LIFT TRAINER. Classified as Device, Biofeedback (product code HCC), Class II - Special Controls.

Submitted by Physical Health Devices, Inc. (Pomano Beach, US). The FDA issued a Cleared decision on January 3, 1990 after a review of 336 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 882.5050 - the FDA neurology 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. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the Neurology review framework, consistent with the majority of Class II 510(k) submissions.

View all Physical Health Devices, Inc. devices

FDA 510(k) Submission Details - K890500

510(k) Number K890500 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 01, 1989
Decision Date January 03, 1990
Days to Decision 336 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
188d slower than avg
Panel avg: 148d · This submission: 336d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HCC Device Classification - Class 2, Special Controls

Product Code HCC Device, Biofeedback
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 882.5050
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 Neurology devices follow this clearance model.

Regulatory Peers - HCC Device, Biofeedback

All 22
Devices cleared under the same product code (HCC) and FDA review panel - the closest regulatory comparables to K890500.
MYOTRAC+/S, MYODAC+/S
K913898 · Thought Technology , Ltd. · Mar 1992
FLEXCOMP DSP & PROCOMP
K903497 · Thought Technology , Ltd. · Feb 1991
M(3):MICRO MUSCLE MONITOR
K896409 · Thought Technology , Ltd. · Oct 1990
MYODAC2 BIOFEEDBACK DEVICE
K894840 · Thought Technology , Ltd. · Oct 1989
MYODAC
K883597 · Thought Technology , Ltd. · Nov 1988
MYOTRAC
K881416 · Thought Technology , Ltd. · Sep 1988