Baxter Healthcare Corp

Baxter Healthcare Corp holds 505 FDA 510(k) medical device clearances, first cleared 1977, most recent 2019, with 86 FDA device recalls on record.

Clearances by Baxter Healthcare Corp — page 6

501–505 of 505

K802166 — MODEL AS* 7B AUTOSYRINGE INFUSION PUMPCode FLN·1980-11-12
K791566 — MODEL AS* 6C INFUSION PUMPCode FRW·1979-11-13
K782034 — INFUSION PUMP, MODEL AS*5Code FRN·1979-02-27
K781036 — AUTO-SYRINGE INFUSION SETCode FPA·1978-08-10
K761307 — AUTO SYRINGE MODEL AS-3ACode FRN·1977-01-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.