K-number	K832912
Device name	GELENDER VACUUM FIXATION RING SYS
Applicant	Miami Eye Technology, Inc.
Product code	HNH
Device class	Class I
Decision date	Jan 10, 1984
Decision	Substantially Equivalent
Regulation	886.4350

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View the full FDA submission: accessdata.fda.gov

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GELENDER VACUUM FIXATION RING SYS

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