K-number	K062335
Device name	SEDECAL X PLUS LP PLUS
Applicant	Sedecal., Sa.
Product code	KPR
Device class	Class II
Decision date	Sep 14, 2006
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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SEDECAL X PLUS LP PLUS

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