ZEST ANCHOR ADVANCED GENERATION— 510(k) K925700

Name: FDA 510(k) clearance K925700
Creator: U.S. Food and Drug Administration
Published: 1994-04-07

Substantially Equivalent

Zest Anchors, Inc.

FDA 510(k) clearance K925700 for ZEST ANCHOR ADVANCED GENERATION, Substantially Equivalent on 1994-04-07. Applicant: Zest Anchors, Inc.. Device class: 1.

Clearance details

Applicant: Zest Anchors, Inc.
Product code: Code EGG
Device class: Class 1
Regulation: 21 CFR 872.3165
Advisory panel: Dental
Date received: 1992-11-12
Decision date: 1994-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Escondido, CA, US

Download summary PDF View on FDA.gov ↗

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