Cleared Traditional

930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES

K851718 · Artiberia · Dental
Jul 1985
Decision
68d
Days
Class 1
Risk

About This 510(k) Submission

K851718 is an FDA 510(k) clearance for the 930/0 TO 950/6 VARIOUS TYPES OF BONE CURETTES, a Curette, Surgical, Dental (Class I — General Controls, product code EMK), submitted by Artiberia (San Antonio, US). The FDA issued a Cleared decision on July 2, 1985, 68 days after receiving the submission on April 25, 1985. This device falls under the Dental review panel. Regulated under 21 CFR 872.4565.

Submission Details

510(k) Number K851718 FDA.gov
FDA Decision Cleared SESE
Date Received April 25, 1985
Decision Date July 02, 1985
Days to Decision 68 days
Submission Type Traditional
Review Panel Dental (DE)
Summary —

Device Classification

Product Code EMK — Curette, Surgical, Dental
Device Class Class I — General Controls
CFR Regulation 21 CFR 872.4565