Cleared Traditional

K010195 - PREMIER ULTRASONIC SCALER AND INSERTS

K010195 is an FDA 510(k) clearance for PREMIER ULTRASONIC SCALER AND INSERTS, manufactured by Premier Dental Products Co.. The device is a Class 2 Dental device with product code ELC cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K010195 · Premier Dental Products Co. · Dental device
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Apr 2001
Decision
85d
Days
Class 2
Risk

K010195 is an FDA 510(k) clearance for the PREMIER ULTRASONIC SCALER AND INSERTS. Classified as Scaler, Ultrasonic (product code ELC), Class II - Special Controls.

Submitted by Premier Dental Products Co. (King Of Prussia, US). The FDA issued a Cleared decision on April 17, 2001 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4850 - 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 Premier Dental Products Co. devices

FDA 510(k) Submission Details - K010195

510(k) Number K010195 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 2001
Decision Date April 17, 2001
Days to Decision 85 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
42d faster than avg
Panel avg: 127d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ELC Device Classification - Class 2, Special Controls

Product Code ELC Scaler, Ultrasonic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.4850
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 - ELC Scaler, Ultrasonic

All 82
Devices cleared under the same product code (ELC) and FDA review panel - the closest regulatory comparables to K010195.
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