K-number	K913273
Device name	DROLITE(TM) LIGHT SOURCE
Applicant	Vision Medical, Inc.
Product code	HJM
Device class	Class II
Decision date	Dec 4, 1991
Decision	Substantially Equivalent
Regulation	886.1945

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Source

View the full FDA submission: accessdata.fda.gov

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DROLITE(TM) LIGHT SOURCE

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