K-number	K854873
Device name	INTRAOCULAR PRESSURE REDUCER
Applicant	Mira, Inc.
Product code	LCR
Device class	Class II
Decision date	Feb 4, 1986
Decision	Substantially Equivalent
Regulation	862.3900

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Source

View the full FDA submission: accessdata.fda.gov

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INTRAOCULAR PRESSURE REDUCER

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