CITRASATE DIALYSATE ACID CONCENTRATE LIQUID, MODELS CS-1XXX-XX, CS-XXX-XX, CS-3XXX-XX (K000792) — FDA 510(k) Clearance | Predicase

K-number	K000792
Device name	CITRASATE DIALYSATE ACID CONCENTRATE LIQUID, MODELS CS-1XXX-XX, CS-XXX-XX, CS-3XXX-XX
Applicant	Advanced Renal Technologies, Inc.
Product code	KPO
Device class	Class II
Decision date	Jun 8, 2000
Decision	Substantially Equivalent
Regulation	876.5820

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View the full FDA submission: accessdata.fda.gov

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