Medisystems Corp.
Medisystems Corp. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 2007.
Top product codes for Medisystems Corp.
Recent clearances by Medisystems Corp.
- K062953 — MEDISYSTEMS ARTERIAL-VENOUS FISTULA NEEDLE SET WITH SECUREMENT DEVICE
- K010279 — MEDISYSTEMS LUER ACCESS INJECTION SITE
- K002372 — ACCESS ALERT GAUGE
- K994306 — REVERSO
- K990803 — MEDISYSTEMS BUTTONHOLE NEEDLE SETS
- K983076 — MEDISYSTEMS TRANSDUCER PROTECTOR
- K971860 — MEDISYSTEMS DIALYSIS PRIMING SETS
- K963668 — MEDISYSTEMS PERITONEAL DIALYSIS SETS
- K970536 — MEDISYSTEMS TRANDUCER PROTECTOR
- K953823 — ARTERIAL VENOUS BLOOD TUBING SET
- K932074 — MEDISYSTEMS APHERESIS NEEDLE WITH GUARD
- K910734 — MEDISYSTEMS HEMODIALYSIS FISTULA SET
- K910733 — MEDISYSTEMS ANTI-STICK INJECTION SITE NEEDLE
- K895856 — MEDISYSTEMS TRANSDUCER PROTECTOR
- K862002 — MEDISYSTEMS PHERESIS NEEDLE
- K823068 — MEDISYSTEMS FISTULA NEEDLES
- K823069 — KF-E SERIES HOLLOW FIBER DIALYZER
- K812910 — MEDISYSTEMS NEEDLES & SYRINGES
- K812353 — KF-E SERIES OF HOLLOW FIBER DIALYZERS
- K811838 — MEDISYSTEMS FISTULA NEEDLE
- K811839 — MEDISYSTEM NEGATIVE PRESSURE
- K811837 — I.V. ADMINISTRATION SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.