Cleared Traditional

ZEST ANCHOR ADVANCED GENERATION

K925700 · Zest Anchors, Inc. · Dental
Apr 1994
Decision
511d
Days
Class 1
Risk

About This 510(k) Submission

K925700 is an FDA 510(k) clearance for the ZEST ANCHOR ADVANCED GENERATION, a Attachment, Precision, All (Class I — General Controls, product code EGG), submitted by Zest Anchors, Inc. (Escondido, US). The FDA issued a Cleared decision on April 7, 1994, 511 days after receiving the submission on November 12, 1992. This device falls under the Dental review panel. Regulated under 21 CFR 872.3165.

Submission Details

510(k) Number K925700 FDA.gov
FDA Decision Cleared SESE
Date Received November 12, 1992
Decision Date April 07, 1994
Days to Decision 511 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code EGG — Attachment, Precision, All
Device Class Class I — General Controls
CFR Regulation 21 CFR 872.3165

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