K-number	K802286
Device name	ARGLE LATEX PENROSE TUBING
Applicant	Sherwood Medical Co.
Product code	KGZ
Device class	Class I
Decision date	Oct 23, 1980
Decision	Substantially Equivalent
Regulation	878.4200

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View the full FDA submission: accessdata.fda.gov

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ARGLE LATEX PENROSE TUBING

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