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Exelint Intl. Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K092172EXEL I.V. EXTENSION SETJanuary 4, 2010
K052103EXEL SECURE TOUCH II SAFETY SYRINGEOctober 19, 2005
K031500EXCEL PRIMARY SOLUTION SETJuly 25, 2003
K011754EXEL SECURETOUCH PTP SYRINGEJanuary 22, 2003
K020533EXEL VACULET BLOOD COLLECTION SETDecember 2, 2002
K022406EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SETSeptember 30, 2002
K011757EXEL COMFORTPOINT INSULIN PEN NEEDLEJanuary 23, 2002
K012879EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITEJanuary 17, 2002
K013037EXCEL A.V FISUTAL NEEDLE SETDecember 7, 2001
K011405EXEL INJECTION PLUG WITH CAPSeptember 27, 2001
K010404EXEL I.V. ADMINISTRATION SETAugust 30, 2001
K992039EXEL I.V. BLOOD LINE SETFebruary 10, 2000