Exel Intl.
Exel Intl. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2000.
Top product codes for Exel Intl.
Recent clearances by Exel Intl.
- K992290 — EXEL INJECTION PLUG WITH CAP
- K963658 — EXEL AVF SINGLE NEEDLE
- K963659 — EXEL I.V. ADMINISTRATION SET
- K926119 — EXEL HUBER INFUSION SET ROTATING WING
- K904685 — EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)
- K903945 — EXEL A-V FISTULA SET
- K895770 — EXEL HUBER INFUSION SET
- K895768 — EXEL SAFELET CATHETER
- K895769 — EXEL HUBER NEEDLE
- K895771 — EXEL SPINAL NEEDLES
- K895772 — EXEL INDWELLING CATHETER
- K862492 — EXEL THREE-WAY STOPCOCK
- K861449 — VACUUM BLOOD COLLECTING SYSTEM (NEO-TUBE)
- K862491 — EXEL BUTTERFLY SCALP VEIN SET
- K861152 — EXEL VACUUM BLOOD COLLECTING SYSTEM
- K861153 — DISPOSABLE SYRINGES AND HYPODERMIC NEEDLES
- K861151 — SUEL BLOOD LANCET
- K861150 — EXEL DENTAL NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.