K-number	K820431
Device name	E.R.C.P. CANNULAS
Applicant	American Endoscopy, Inc.
Product code	ODD
Device class	Class II
Decision date	Apr 9, 1982
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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E.R.C.P. CANNULAS

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