Cleared Traditional

K932886 - ALPHA-DENT LIGHT ACTIVATED CORE BUILDUP...

K932886 is the FDA 510(k) clearance for ALPHA-DENT LIGHT ACTIVATED CORE BUILDUP... by Wallace A. Erickson & Co.. It is a Class 2 Dental device (product code EBF) cleared through the Traditional 510(k) pathway after a 107-day FDA review.

K932886 · Wallace A. Erickson & Co. · Dental device
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Sep 1993
Decision
107d
Days
Class 2
Risk

K932886 is an FDA 510(k) clearance for the ALPHA-DENT LIGHT ACTIVATED CORE BUILDUP BLUE PASTE. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Wallace A. Erickson & Co. (Chicago, US). The FDA issued a Cleared decision on September 29, 1993 after a review of 107 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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 Wallace A. Erickson & Co. devices

Submission Details

510(k) Number K932886 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 14, 1993
Decision Date September 29, 1993
Days to Decision 107 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
20d faster than avg
Panel avg: 127d · This submission: 107d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
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 - EBF Material, Tooth Shade, Resin

All 578
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K932793 · Pulpdent Corp. · Sep 1993