Cleared Traditional

K113430 - PROULTRA PIEZO ULTRASONIC

K113430 is an FDA 510(k) clearance for PROULTRA PIEZO ULTRASONIC, manufactured by Satelec - Acteon Group. The device is a Class 2 Dental device with product code ELC cleared through the Traditional 510(k) pathway after a 94-day FDA review.

K113430 · Satelec - Acteon Group · Dental device
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Feb 2012
Decision
94d
Days
Class 2
Risk

K113430 is an FDA 510(k) clearance for the PROULTRA PIEZO ULTRASONIC. Classified as Scaler, Ultrasonic (product code ELC), Class II - Special Controls.

Submitted by Satelec - Acteon Group (Mt. Laurel, US). The FDA issued a Cleared decision on February 23, 2012 after a review of 94 days - within the typical 510(k) review window.

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: 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 Satelec - Acteon Group devices

FDA 510(k) Submission Details - K113430

510(k) Number K113430 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 21, 2011
Decision Date February 23, 2012
Days to Decision 94 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
33d faster than avg
Panel avg: 127d · This submission: 94d
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 79
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