K-number	K930474
Device name	NEEDLE, PNEUMOPERITONEUM, SPRING LOADED
Applicant	Ranfac, Corp.
Product code	FHO
Device class	Class II
Decision date	Jul 23, 1993
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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NEEDLE, PNEUMOPERITONEUM, SPRING LOADED

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