K-number	K973955
Device name	HERNIAMESH SURGICAL MESHES
Applicant	Herniamesh
Product code	FTL
Device class	Class II
Decision date	May 11, 1998
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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HERNIAMESH SURGICAL MESHES

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