K-number	K043130
Device name	MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS
Applicant	Pajunk GmbH
Product code	CAZ
Device class	Class II
Decision date	Dec 21, 2004
Decision	Substantially Equivalent
Regulation	868.5140

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO PAJUNK STIMULONG PLUS CATHETER SETS

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