K-number	K203505
Device name	DORO QR3 Headrest System (Aluminum)
Applicant	Pro Med Instruments GmbH
Product code	HBL
Device class	Class II
Decision date	Mar 29, 2021
Decision	Substantially Equivalent
Regulation	882.4460

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View the full FDA submission: accessdata.fda.gov

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DORO QR3 Headrest System (Aluminum)

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