Cleared Traditional

600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI

K851712 · Artiberia · Dental
Jun 1985
Decision
47d
Days
Class 1
Risk

About This 510(k) Submission

K851712 is an FDA 510(k) clearance for the 600/203 TO 650/74XN VARIOUS TYPES OF DENT EXTRACTI, a Forceps, Tooth Extractor, Surgical (Class I — General Controls, product code EMG), submitted by Artiberia (San Antonio, US). The FDA issued a Cleared decision on June 11, 1985, 47 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 K851712 FDA.gov
FDA Decision Cleared SESE
Date Received April 25, 1985
Decision Date June 11, 1985
Days to Decision 47 days
Submission Type Traditional
Review Panel Dental (DE)
Summary —

Device Classification

Product Code EMG — Forceps, Tooth Extractor, Surgical
Device Class Class I — General Controls
CFR Regulation 21 CFR 872.4565

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