K-number	K912724
Device name	GUIDOR(TM)
Applicant	Procordia Oratech AB
Product code	NPK
Device class	Class II
Decision date	May 13, 1993
Decision	Substantially Equivalent for Some Indications
Regulation	872.3930

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View the full FDA submission: accessdata.fda.gov

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GUIDOR(TM)

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