K-number	K791703
Device name	TEW BYPASS INSTRUMENTS & DISSECTING KIT
Applicant	Edward Weck, Inc.
Product code	GDI
Device class	Class I
Decision date	Oct 4, 1979
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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TEW BYPASS INSTRUMENTS & DISSECTING KIT

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