Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Parker Hannifin Corp.

FDA 510(k) & PMA Approved Devices — 8 products

Total Devices8
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K161731 Cleveland Multiport Ventricular Catheter SetHCA2017-03-27 View
510(k) K897086 PARKER AMBULATORY MEDICATION INFUSION PUMP 2004FRN1990-09-28 View
510(k) K863532 MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSERFRN1987-01-14 View
510(k) K834461 INFUSION PUMP PRIMERFRN1984-01-30 View
510(k) K833723 MODEL 2000 AMBULATORY MED. INFUSERFRN1984-01-30 View
510(k) K831402 PRESSURE MONITOR & CONTROL UNIT APC-02AKXM1983-08-08 View
510(k) K831747 PLASMA THERAPY TUBESET-E100 SERIESFJK1983-06-30 View
510(k) K830818 ASAHI BLOOD/PLASMA PUMP #ABP-01A &FIR1983-04-12 View
↑