Cleared Traditional

K862912 - RENAMELIZE POLISHING PASTE (FDA 510(k) Clearance)

Aug 1986
Decision
11d
Days
Class 1
Risk

K862912 is an FDA 510(k) clearance for the RENAMELIZE POLISHING PASTE. This device is classified as a Agent, Polishing, Abrasive, Oral Cavity (Class I - General Controls, product code EJR).

Submitted by Cosmedent, Inc. (Chicago, US). The FDA issued a Cleared decision on August 12, 1986, 11 days after receiving the submission on August 1, 1986.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6030.

Submission Details

510(k) Number K862912 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 01, 1986
Decision Date August 12, 1986
Days to Decision 11 days
Submission Type Traditional
Review Panel Dental (DE)
Summary

Device Classification

Product Code EJR — Agent, Polishing, Abrasive, Oral Cavity
Device Class Class I - General Controls
CFR Regulation 21 CFR 872.6030