K-number	K191979
Device name	DORO QR3 XTom Headholder System
Applicant	Pro Med Instruments GmbH
Product code	HBL
Device class	Class II
Decision date	Oct 22, 2019
Decision	Substantially Equivalent
Regulation	882.4460

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View the full FDA submission: accessdata.fda.gov

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DORO QR3 XTom Headholder System

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