K-number	K770503
Device name	LOUISVILLE CLAMP PRODUCT #65-172
Applicant	Edward Weck, Inc.
Product code	DXC
Device class	Class II
Decision date	Mar 30, 1977
Decision	Substantially Equivalent
Regulation	870.4450

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View the full FDA submission: accessdata.fda.gov

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LOUISVILLE CLAMP PRODUCT #65-172

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