K-number	K905299
Device name	ROMFLEX REHABILITATION EQUIPMENT
Applicant	Dyna Flex, Intl.
Product code	BXB
Device class	Class I
Decision date	Dec 31, 1990
Decision	Substantially Equivalent
Regulation	890.5380

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View the full FDA submission: accessdata.fda.gov

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ROMFLEX REHABILITATION EQUIPMENT

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