Cleared Traditional

K024046 - TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P (FDA 510(k) Clearance)

Feb 2003
Decision
62d
Days
Class 2
Risk

K024046 is an FDA 510(k) clearance for the TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P. This device is classified as a Coating, Filling Material, Resin (Class II - Special Controls, product code EBD).

Submitted by Bisco, Inc. (Schaumburg, US). The FDA issued a Cleared decision on February 6, 2003, 62 days after receiving the submission on December 6, 2002.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3310.

Submission Details

510(k) Number K024046 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 06, 2002
Decision Date February 06, 2003
Days to Decision 62 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code EBD — Coating, Filling Material, Resin
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.3310