K-number	K840181
Device name	CATAREX/ULTRASONICS KIT
Applicant	Calliope Corp.
Product code	HQC
Device class	Class II
Decision date	Oct 5, 1984
Decision	Substantially Equivalent
Regulation	886.4670

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View the full FDA submission: accessdata.fda.gov

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CATAREX/ULTRASONICS KIT

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