K-number	K010305
Device name	WEISS RETINAL CANNULA
Applicant	Micron Surgical, Inc.
Product code	HMX
Device class	Class I
Decision date	May 2, 2001
Decision	Substantially Equivalent
Regulation	886.4350

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View the full FDA submission: accessdata.fda.gov

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WEISS RETINAL CANNULA

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