K-number	K974813
Device name	COMBISON 530D WITH POWER DOPPLER MODE
Applicant	Medison America, Inc.
Product code	IYN
Device class	Class II
Decision date	Sep 29, 1998
Decision	Substantially Equivalent
Regulation	892.1550

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View the full FDA submission: accessdata.fda.gov

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COMBISON 530D WITH POWER DOPPLER MODE

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