HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P— 510(k) K102305

Name: FDA 510(k) clearance K102305
Creator: U.S. Food and Drug Administration
Published: 2010-12-03

Substantially Equivalent

Hass Corp.

FDA 510(k) clearance K102305 for HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P, Substantially Equivalent on 2010-12-03. Applicant: Hass Corp.. Device class: 2.

Clearance details

Applicant: Hass Corp.
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2010-08-16
Decision date: 2010-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, 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.