K-number	K902983
Device name	SIEMEN'S SIREMOBILE II C-ARM
Applicant	Electromek Diagnostic Systems, Inc.
Product code	JAA
Device class	Class II
Decision date	Nov 6, 1990
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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SIEMEN'S SIREMOBILE II C-ARM

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