Gainor Medical Europe, Ltd.
Gainor Medical Europe, Ltd. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1994.
Top product codes for Gainor Medical Europe, Ltd.
Recent clearances by Gainor Medical Europe, Ltd.
- K926448 — I.V. ADMINISTRATION SET
- K931828 — CARELET SAFETY LANCET
- K931827 — CLEANLET, CLEANLET XL & KIDS
- K922441 — SURESEAL BANDAGE
- K913333 — I.V. PRIMING SET
- K902422 — NEEDLE, ASPIRATION & INJECTION, DISPOSABLE
- K902420 — CATHETER, NASAL, OXYGEN
- K902564 — NEEDLE, DIALYSIS
- K902421 — STOMACH, GASTRO-ENTEROSTOMY
- K902426 — HEMODIALYSIS SYSTEM AND ACCESSORY
- K902416 — SURELITE AND SURELITE XL BLOOD LANCET
- K902417 — BAG, URINE
- K900306 — HEMODIALYSIS BLOOD LINES
Data sourced from openFDA. This site is unofficial and independent of the FDA.