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Exel Intl.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992290EXEL INJECTION PLUG WITH CAPFebruary 23, 2000
K963658EXEL AVF SINGLE NEEDLEMay 5, 1998
K963659EXEL I.V. ADMINISTRATION SETDecember 16, 1997
K926119EXEL HUBER INFUSION SET ROTATING WINGAugust 11, 1993
K904685EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)November 21, 1990
K903945EXEL A-V FISTULA SETNovember 20, 1990
K895770EXEL HUBER INFUSION SETJuly 19, 1990
K895771EXEL SPINAL NEEDLESFebruary 16, 1990
K895772EXEL INDWELLING CATHETERFebruary 16, 1990
K895768EXEL SAFELET CATHETERFebruary 16, 1990
K895769EXEL HUBER NEEDLEFebruary 16, 1990
K862492EXEL THREE-WAY STOPCOCKSeptember 25, 1986
K861449VACUUM BLOOD COLLECTING SYSTEM (NEO-TUBE)September 16, 1986
K862491EXEL BUTTERFLY SCALP VEIN SETAugust 27, 1986
K861152EXEL VACUUM BLOOD COLLECTING SYSTEMMay 6, 1986
K861153DISPOSABLE SYRINGES AND HYPODERMIC NEEDLESApril 23, 1986
K861151SUEL BLOOD LANCETApril 15, 1986
K861150EXEL DENTAL NEEDLEApril 11, 1986