K-number	K812219
Device name	MODEL 900S INTRAOCULAR PROBE
Applicant	Lumenis, Inc.
Product code	HQF
Device class	Class II
Decision date	Nov 16, 1981
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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MODEL 900S INTRAOCULAR PROBE

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