Cleared Traditional

K893255 - SPECTRUM, VISIBLE LIGHT CURE ORTHODONTIC ADHESIVE (FDA 510(k) Clearance)

Jun 1989
Decision
54d
Days
Class 2
Risk

K893255 is an FDA 510(k) clearance for the SPECTRUM, VISIBLE LIGHT CURE ORTHODONTIC ADHESIVE. This device is classified as a Adhesive, Bracket And Tooth Conditioner, Resin (Class II - Special Controls, product code DYH).

Submitted by American Orthodontics (Sheboygan, US). The FDA issued a Cleared decision on June 21, 1989, 54 days after receiving the submission on April 28, 1989.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3750.

Submission Details

510(k) Number K893255 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 28, 1989
Decision Date June 21, 1989
Days to Decision 54 days
Submission Type Traditional
Review Panel Dental (DE)
Summary

Device Classification

Product Code DYH — Adhesive, Bracket And Tooth Conditioner, Resin
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.3750