K-number	K901441
Device name	ALBERT MORTON UROLOGICAL CATHETER
Applicant	Transinternational Marketing Group
Product code	GBM
Device class	Class II
Decision date	Jun 22, 1990
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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ALBERT MORTON UROLOGICAL CATHETER

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