K-number	K924968
Device name	L-CATH PEEL-AWAY CATHETER SYSTEM
Applicant	Luther Medical Products, Inc.
Product code	FOZ
Device class	Class II
Decision date	May 21, 1993
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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L-CATH PEEL-AWAY CATHETER SYSTEM

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