Cleared Traditional

C & B 40 PENTRO C & B40 (K833290) - FDA 510(k) Clearance

Class I Dental device.

K833290 · Genesis Industries, Inc. · Dental device
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Jan 1984
Decision
103d
Days
Class 1
Risk

K833290 is an FDA 510(k) clearance for the C & B 40 PENTRO C & B40. Classified as Remover, Crown (product code EIS), Class I - General Controls.

Submitted by Genesis Industries, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 3, 1984 after a review of 103 days - within the typical 510(k) review window.

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. 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 Genesis Industries, Inc. devices

Submission Details

510(k) Number K833290 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 1983
Decision Date January 03, 1984
Days to Decision 103 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
24d faster than avg
Panel avg: 127d · This submission: 103d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EIS Remover, Crown
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.