K-number	K961078
Device name	AUTOMATED VITRECTOMY DEVICE
Applicant	Promex, Inc.
Product code	HQE
Device class	Class II
Decision date	Jun 14, 1996
Decision	Substantially Equivalent
Regulation	886.4150

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Source

View the full FDA submission: accessdata.fda.gov

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AUTOMATED VITRECTOMY DEVICE

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