K-number	K811658
Device name	ANIS LENS IMPLANT FORCEPS #2
Applicant	American V. Mueller
Product code	HNR
Device class	Class I
Decision date	Jun 26, 1981
Decision	Substantially Equivalent
Regulation	886.4350

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View the full FDA submission: accessdata.fda.gov

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ANIS LENS IMPLANT FORCEPS #2

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