DENTIN RELIEF— 510(k) K924670

Substantially Equivalent

Professional Technologies Corp.

FDA 510(k) clearance K924670 for DENTIN RELIEF, Substantially Equivalent on 1992-11-23. Applicant: Professional Technologies Corp.. Device class: 2.

Clearance details

Applicant: Professional Technologies Corp.
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 1992-09-16
Decision date: 1992-11-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ithaca, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KLE

K260485 — Any-Etch2026-05-14
K260430 — Porcelain Etch Gel2026-04-10
K252450 — Adhese 22026-03-05
K260682 — Bond-PR Universal Adhesive2026-03-03
K251587 — VITA VMLC Primer2026-02-23

More clearances from Professional Technologies Corp.

K884012 — MMAC II TONOMETER1989-01-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.