K-number	K052141
Device name	STRYKER STILETTO ELECTROSURGICAL PROBE
Applicant	Stryker Endoscopy
Product code	GEI
Device class	Class II
Decision date	Oct 6, 2005
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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STRYKER STILETTO ELECTROSURGICAL PROBE

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