K-number	K953452
Device name	KETOREX C SANWA
Applicant	Ihara Medics U.S., Inc.
Product code	JMK
Device class	Class I
Decision date	May 2, 1996
Decision	Substantially Equivalent
Regulation	862.1380

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View the full FDA submission: accessdata.fda.gov

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KETOREX C SANWA

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