Cleared Traditional

K850082 - HAND HELD GONIOMETER

K850082 is an FDA 510(k) clearance for HAND HELD GONIOMETER, manufactured by Chattanooga Group, Inc.. The device is a Class 1 Neurology device with product code KQW cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K850082 · Chattanooga Group, Inc. · Neurology device
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Apr 1985
Decision
84d
Days
Class 1
Risk

K850082 is an FDA 510(k) clearance for the HAND HELD GONIOMETER. Classified as Goniometer, Nonpowered (product code KQW), Class I - General Controls.

Submitted by Chattanooga Group, Inc. (Red Bank, US). The FDA issued a Cleared decision on April 4, 1985 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Neurology FDA review panel, regulated under 21 CFR 888.1520 - 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 Chattanooga Group, Inc. devices

FDA 510(k) Submission Details - K850082

510(k) Number K850082 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 10, 1985
Decision Date April 04, 1985
Days to Decision 84 days
Submission Type Traditional
Review Panel Neurology (NE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
64d faster than avg
Panel avg: 148d · This submission: 84d
Pathway characteristics
Predicate-based equivalence.

KQW Device Classification - Class 1, General Controls

Product Code KQW Goniometer, Nonpowered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 888.1520
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 - KQW Goniometer, Nonpowered

All 9
Devices cleared under the same product code (KQW) and FDA review panel - the closest regulatory comparables to K850082.
DOBBHOFF(R) RETRIEVAL FORCEPS
K901744 · Biosearch Medical Products, Inc. · Jul 1990
FINGER BONIOMETER BK7506
K831550 · Fred Sammons, Inc. · Jun 1983
UNIVERSAL GONIMETER
K810441 · Fred Sammons, Inc. · Feb 1981
BK-7497 BULB DYNAMOMETER
K801715 · Fred Sammons, Inc. · Aug 1980
BK-7505 RADIOPAQUE GONIOMETER, 8
K801716 · Fred Sammons, Inc. · Aug 1980
BK-7511 BRASS GONIOMETER
K801717 · Fred Sammons, Inc. · Aug 1980