K-number	K904694
Device name	CUSTOMED ANGIODRAPE PACK FEMORAL
Applicant	Customed, Inc.
Product code	KKX
Device class	Class II
Decision date	Jan 2, 1991
Decision	Unknown
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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CUSTOMED ANGIODRAPE PACK FEMORAL

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