K-APATITE 20-40 MESH K-APATITE 40-60— 510(k) K843557

Name: FDA 510(k) clearance K843557
Creator: U.S. Food and Drug Administration
Published: 1984-11-30

Substantially Equivalent

Katecho, Inc.

FDA 510(k) clearance K843557 for K-APATITE 20-40 MESH K-APATITE 40-60, Substantially Equivalent on 1984-11-30. Applicant: Katecho, Inc.. Device class: 2.

Clearance details

Applicant: Katecho, Inc.
Product code: Code ELE
Device class: Class 2
Regulation: 21 CFR 872.3645
Advisory panel: Dental
Date received: 1984-09-10
Decision date: 1984-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Des Moines, IA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.