Exelint Intl. Co.
Exelint Intl. Co. appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 4, 2010.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K092172 | EXEL I.V. EXTENSION SET | January 4, 2010 |
| K052103 | EXEL SECURE TOUCH II SAFETY SYRINGE | October 19, 2005 |
| K031500 | EXCEL PRIMARY SOLUTION SET | July 25, 2003 |
| K011754 | EXEL SECURETOUCH PTP SYRINGE | January 22, 2003 |
| K020533 | EXEL VACULET BLOOD COLLECTION SET | December 2, 2002 |
| K022406 | EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET | September 30, 2002 |
| K011757 | EXEL COMFORTPOINT INSULIN PEN NEEDLE | January 23, 2002 |
| K012879 | EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE | January 17, 2002 |
| K013037 | EXCEL A.V FISUTAL NEEDLE SET | December 7, 2001 |
| K011405 | EXEL INJECTION PLUG WITH CAP | September 27, 2001 |
| K010404 | EXEL I.V. ADMINISTRATION SET | August 30, 2001 |
| K992039 | EXEL I.V. BLOOD LINE SET | February 10, 2000 |