K-number	K062308
Device name	LMT-KATH-S; LMT-KATH-I
Applicant	Licher Medizintechnologie GmbH
Product code	FPA
Device class	Class II
Decision date	Mar 20, 2007
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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LMT-KATH-S; LMT-KATH-I

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