K-number	K973028
Device name	HELIOS LASER IMAGER 1417
Applicant	Sterling Diagnostic Imaging, Inc.
Product code	LMC
Device class	Class II
Decision date	Oct 28, 1997
Decision	Substantially Equivalent
Regulation	892.2040

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View the full FDA submission: accessdata.fda.gov

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HELIOS LASER IMAGER 1417

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