Cleared Traditional

K923902 - STERILE DENTAL KITS

K923902 is an FDA 510(k) clearance for STERILE DENTAL KITS, manufactured by Professional Sterile Systems, Inc.. The device is a Class 1 Dental device with product code EKJ cleared through the Traditional 510(k) pathway after a 329-day FDA review.

K923902 · Professional Sterile Systems, Inc. · Dental device
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Jun 1993
Decision
329d
Days
Class 1
Risk

K923902 is an FDA 510(k) clearance for the STERILE DENTAL KITS. Classified as Burnisher, Operative (product code EKJ), Class I - General Controls.

Submitted by Professional Sterile Systems, Inc. (Lawrenceville, US). The FDA issued a Cleared decision on June 29, 1993 after a review of 329 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4565 - 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. Elevated predicate reliance profile. 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 Professional Sterile Systems, Inc. devices

FDA 510(k) Submission Details - K923902

510(k) Number K923902 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 1992
Decision Date June 29, 1993
Days to Decision 329 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
202d slower than avg
Panel avg: 127d · This submission: 329d
Pathway characteristics
Predicate-based equivalence.

EKJ Device Classification - Class 1, General Controls

Product Code EKJ Burnisher, Operative
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.4565
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 - EKJ Burnisher, Operative

All 23
Devices cleared under the same product code (EKJ) and FDA review panel - the closest regulatory comparables to K923902.
PRESTERILIZED ENDODONTIC FILES
K943584 · Dentsply Intl. · Sep 1994
AMD DENTIST AND HYGIENIST KITS
K925115 · Advance Medical Designs, Inc. · Jul 1994
APPLICATOR NOZZLE
K926368 · Centrix, Inc. · Sep 1993
PART 872 DEGUFILL H & DEGUFILL M DA
K914368 · Degussa AG · Nov 1991
IMPLARETTE
K911655 · Implant Innovations International, Inc. · Oct 1991
HARDCOATED PLASTIC FILLING INSTRUMENT
K912149 · Premier Dental Products Co. · Jun 1991