Cleared Traditional

K984415 - S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F

K984415 is an FDA 510(k) clearance for S.S. WHITE TECHNOLOGIES, manufactured by S.S. White Technologies, Inc.. The device is a Class 2 Dental device with product code KOJ cleared through the Traditional 510(k) pathway after a 293-day FDA review.

K984415 · S.S. White Technologies, Inc. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1999
Decision
293d
Days
Class 2
Risk

K984415 is an FDA 510(k) clearance for the S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F. Classified as Airbrush (product code KOJ), Class II - Special Controls.

Submitted by S.S. White Technologies, Inc. (Piscataway, US). The FDA issued a Cleared decision on September 29, 1999 after a review of 293 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6080 - the FDA dental device regulatory 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 Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all S.S. White Technologies, Inc. devices

FDA 510(k) Submission Details - K984415

510(k) Number K984415 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 10, 1998
Decision Date September 29, 1999
Days to Decision 293 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
166d slower than avg
Panel avg: 127d · This submission: 293d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KOJ Device Classification - Class 2, Special Controls

Product Code KOJ Airbrush
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.6080
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 Dental devices follow this clearance model.

Regulatory Peers - KOJ Airbrush

All 28
Devices cleared under the same product code (KOJ) and FDA review panel - the closest regulatory comparables to K984415.
KAVO CORUND HANDPIECE 2013
K002708 · Kavo America · Nov 2000
MACH 7
K990060 · Kreativ, Inc. · Jun 2000
SIMPLEX AIRBRATOR (SAB-7)
K980672 · Irt Management Corp. · May 2000
JETSONIC 2000
K990545 · Sds Dental, Inc. · Aug 1999
AIR TECHNIQUES' AIRDENT II
K981564 · Air Techniques, Inc. · Sep 1998
PREPTECH(TM) 200 CAVITY PREPARATION SYSTEM
K974655 · Prep Technology Corp. · Jul 1998