ZEST MARK II (STANDARD & MINI)— 510(k) K861561

Name: FDA 510(k) clearance K861561
Creator: U.S. Food and Drug Administration
Published: 1986-05-21

Substantially Equivalent

Zest Anchors, Inc.

FDA 510(k) clearance K861561 for ZEST MARK II (STANDARD & MINI), Substantially Equivalent on 1986-05-21. 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: 1986-04-25
Decision date: 1986-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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K915299 — COGAN CORP KITS OF DENTAL HAND INSTRUMENTS1992-01-31
K912435 — DENTAL CONNECTOR PRECISION ATTACHMENT1991-08-28

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