K-number	K822551
Device name	AMP CAPD UNISPIKE AMINISTRATION SET
Applicant	American Medical Products, Inc.
Product code	FKK
Device class	Class I
Decision date	Oct 13, 1982
Decision	Substantially Equivalent
Regulation	876.4730

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View the full FDA submission: accessdata.fda.gov

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AMP CAPD UNISPIKE AMINISTRATION SET

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