Cleared Traditional

K884165 - MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS

K884165 is an FDA 510(k) clearance for MUSCLE EXAMINATION & EXERCISE DOSIMETER..., manufactured by Spark Instruments & Academics, Inc.. The device is a Class 2 Neurology device with product code LBB cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K884165 · Spark Instruments & Academics, Inc. · Neurology device
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Oct 1988
Decision
22d
Days
Class 2
Risk

K884165 is an FDA 510(k) clearance for the MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS. Classified as Dynamometer, Ac-powered (product code LBB), Class II - Special Controls.

Submitted by Spark Instruments & Academics, Inc. (Coralville, US). The FDA issued a Cleared decision on October 26, 1988 after a review of 22 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 888.1240 - 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: 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 Spark Instruments & Academics, Inc. devices

FDA 510(k) Submission Details - K884165

510(k) Number K884165 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 04, 1988
Decision Date October 26, 1988
Days to Decision 22 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
126d faster than avg
Panel avg: 148d · This submission: 22d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LBB Device Classification - Class 2, Special Controls

Product Code LBB Dynamometer, Ac-powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.1240
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 - LBB Dynamometer, Ac-powered

All 12
Devices cleared under the same product code (LBB) and FDA review panel - the closest regulatory comparables to K884165.
MEKANIKA'S SPINAL STIFFNESS GAUGE (SSG)
K964933 · Mekanika, Inc. · Feb 1997
DYNAMOMETER
K964685 · John Chatillon & Sons, Inc. · Jan 1997
ELECTRO-GONIOMETER DIAGNOSTIC DEVICE
K901290 · Chattanooga Group, Inc. · Oct 1990
KIN-COM JR
K881388 · Chattanooga Group, Inc. · Apr 1988
DIGITAL GRIP/PINCH STRENGTH METOR
K850697 · Chattanooga Group, Inc. · May 1985
MED-EX
K812899 · Chattanooga Group, Inc. · Nov 1981