K-number	K771866
Device name	TROUTMAN CORNEAL PUNCH
Applicant	Edward Weck, Inc.
Product code	HRH
Device class	Class I
Decision date	Nov 9, 1977
Decision	Substantially Equivalent
Regulation	886.4350

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View the full FDA submission: accessdata.fda.gov

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TROUTMAN CORNEAL PUNCH

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