Cleared Traditional

STERI-LUBE (K942672) - FDA 510(k) Clearance

Class I Dental device.

K942672 · Petroleum Products of America · Dental device
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Jul 1994
Decision
30d
Days
Class 1
Risk

K942672 is an FDA 510(k) clearance for the STERI-LUBE. Classified as Handpiece, Air-powered, Dental (product code EFB), Class I - General Controls.

Submitted by Petroleum Products of America (Scottsdale, US). The FDA issued a Cleared decision on July 6, 1994 after a review of 30 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4200 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Petroleum Products of America devices

Submission Details

510(k) Number K942672 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 06, 1994
Decision Date July 06, 1994
Days to Decision 30 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
97d faster than avg
Panel avg: 127d · This submission: 30d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EFB Handpiece, Air-powered, Dental
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.4200
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 - EFB Handpiece, Air-powered, Dental

All 37
Devices cleared under the same product code (EFB) and FDA review panel - the closest regulatory comparables to K942672.
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PLAQUE-SWEEP
K873209 · Dentsply Intl. · Aug 1987