FDA 510(k) Applications Submitted by HASS CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K111573 06/06/2011 MONOBLOC BM SERIES HASS CORP.
K102305 08/16/2010 HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P HASS CORP.
K160102 01/19/2016 Amber Mill Series and Amber Press Series HASS CORP.
K202952 09/30/2020 Amber Mill Q Series & Amber Mill Direct Series HASS Corp.


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