K-number	K896096
Device name	SOLOSTICK (AMPLATZ DILATOR NEEDLE)
Applicant	Microvena Corp.
Product code	DRE
Device class	Class II
Decision date	Apr 10, 1990
Decision	Substantially Equivalent
Regulation	870.1310

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View the full FDA submission: accessdata.fda.gov

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SOLOSTICK (AMPLATZ DILATOR NEEDLE)

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