K-number	K922186
Device name	HEM-O-LOK -- MODIFICATION
Applicant	Linvatec Corp.
Product code	GDW
Device class	Class II
Decision date	Aug 6, 1992
Decision	Substantially Equivalent
Regulation	878.4750

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View the full FDA submission: accessdata.fda.gov

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HEM-O-LOK -- MODIFICATION

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