Cleared Traditional

K971735 - ACCUDEXA BONE DENSITOMETER

K971735 is an FDA 510(k) clearance for ACCUDEXA BONE DENSITOMETER, manufactured by Schick Technologies, Inc.. The device is a Class 2 Radiology device with product code KGI cleared through the Traditional 510(k) pathway after a 204-day FDA review.

K971735 · Schick Technologies, Inc. · Radiology device
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Dec 1997
Decision
204d
Days
Class 2
Risk

K971735 is an FDA 510(k) clearance for the ACCUDEXA BONE DENSITOMETER. Classified as Densitometer, Bone (product code KGI), Class II - Special Controls.

Submitted by Schick Technologies, Inc. (Rockville, US). The FDA issued a Cleared decision on December 2, 1997 after a review of 204 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1170 - the FDA radiology and imaging software oversight 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. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Schick Technologies, Inc. devices

FDA 510(k) Submission Details - K971735

510(k) Number K971735 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 12, 1997
Decision Date December 02, 1997
Days to Decision 204 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
97d slower than avg
Panel avg: 107d · This submission: 204d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KGI Device Classification - Class 2, Special Controls

Product Code KGI Densitometer, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1170
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 Radiology devices follow this clearance model.

Regulatory Peers - KGI Densitometer, Bone

All 68
Devices cleared under the same product code (KGI) and FDA review panel - the closest regulatory comparables to K971735.
DPX-RX BONE DENSITOMETER
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APOLLO
K972882 · Norland Corp. · Oct 1997
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