Parker Hannifin Corp.
Parker Hannifin Corp. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 2017.
Top product codes for Parker Hannifin Corp.
Recent clearances by Parker Hannifin Corp.
- K161731 — Cleveland Multiport Ventricular Catheter Set
- K897086 — PARKER AMBULATORY MEDICATION INFUSION PUMP 2004
- K863532 — MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSER
- K833723 — MODEL 2000 AMBULATORY MED. INFUSER
- K834461 — INFUSION PUMP PRIMER
- K831402 — PRESSURE MONITOR & CONTROL UNIT APC-02A
- K831747 — PLASMA THERAPY TUBESET-E100 SERIES
- K830818 — ASAHI BLOOD/PLASMA PUMP #ABP-01A &
Data sourced from openFDA. This site is unofficial and independent of the FDA.