Cleared Traditional

K014238 - DELSONIC 2000

K014238 is an FDA 510(k) clearance for DELSONIC 2000, manufactured by Deldent , Ltd.. The device is a Class 2 Dental device with product code ELC cleared through the Traditional 510(k) pathway after a 29-day FDA review.

K014238 · Deldent , Ltd. · Dental device
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Jan 2002
Decision
29d
Days
Class 2
Risk

K014238 is an FDA 510(k) clearance for the DELSONIC 2000. Classified as Scaler, Ultrasonic (product code ELC), Class II - Special Controls.

Submitted by Deldent , Ltd. (Petach Tikvah, IL). The FDA issued a Cleared decision on January 24, 2002 after a review of 29 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 Deldent , Ltd. devices

FDA 510(k) Submission Details - K014238

510(k) Number K014238 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 26, 2001
Decision Date January 24, 2002
Days to Decision 29 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
98d faster than avg
Panel avg: 127d · This submission: 29d
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 116
Devices cleared under the same product code (ELC) and FDA review panel - the closest regulatory comparables to K014238.
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