K-number	K881681
Device name	CYBEX BACK TESTING AND REHABILITATION SYSTEM
Applicant	Cybex
Product code	IKK
Device class	Class II
Decision date	Apr 25, 1990
Decision	Substantially Equivalent
Regulation	890.1925

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View the full FDA submission: accessdata.fda.gov

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CYBEX BACK TESTING AND REHABILITATION SYSTEM

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