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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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