K-number	K182727
Device name	Trident HD Specimen Radiography System
Applicant	Hologic, Inc.
Product code	MWP
Device class	Class II
Decision date	Jan 10, 2019
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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Trident HD Specimen Radiography System

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