K-number	K854906
Device name	PERCUTANEOUS NEPHROSTOMY SETS (OTTO)
Applicant	Angiomed U.S., Inc.
Product code	GBO
Device class	Class I
Decision date	Jan 24, 1986
Decision	Substantially Equivalent
Regulation	878.4200

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View the full FDA submission: accessdata.fda.gov

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PERCUTANEOUS NEPHROSTOMY SETS (OTTO)

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