K-number	K811966
Device name	VISITEC NEEDLE RANGE (GENERAL HOSPITAL)
Applicant	Visitec Co.
Product code	FMI
Device class	Class II
Decision date	Jul 23, 1981
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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VISITEC NEEDLE RANGE (GENERAL HOSPITAL)

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