Exelint Intl. Co. is one of 15076 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Exelint Intl. Co. - FDA 510(k) Cleared Devices
Recent clearances: EXEL I.V. EXTENSION SET, EXEL SECURE TOUCH II SAFETY SYRINGE, EXEL I.V. BLOOD LINE SET
12
Total
12
Cleared
0
Denied
Exelint Intl. Co. has 12 FDA 510(k) cleared general hospital devices. Based in Culver City, US.
Historical record: 12 cleared submissions from 2000 to 2010.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Exelint Intl. Co.
12 devices
Cleared
Jan 04, 2010
EXEL I.V. EXTENSION SET
General Hospital
167d
Cleared
Oct 19, 2005
EXEL SECURE TOUCH II SAFETY SYRINGE
General Hospital
77d
Cleared
Jul 25, 2003
EXCEL PRIMARY SOLUTION SET
General Hospital
73d
Cleared
Jan 22, 2003
EXEL SECURETOUCH PTP SYRINGE
General Hospital
595d
Cleared
Dec 02, 2002
EXEL VACULET BLOOD COLLECTION SET
General Hospital
286d
Cleared
Sep 30, 2002
EXEL SECURETOUCH SAFETY VACULET BLOOD COLLECTION SET
General Hospital
69d
Cleared
Jan 23, 2002
EXEL COMFORTPOINT INSULIN PEN NEEDLE
General Hospital
231d
Cleared
Jan 17, 2002
EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE
General Hospital
142d
Cleared
Dec 07, 2001
EXCEL A.V FISUTAL NEEDLE SET
Gastroenterology & Urology
88d
Cleared
Sep 27, 2001
EXEL INJECTION PLUG WITH CAP
General Hospital
142d
Cleared
Aug 30, 2001
EXEL I.V. ADMINISTRATION SET
General Hospital
199d
Cleared
Feb 10, 2000
EXEL I.V. BLOOD LINE SET
Gastroenterology & Urology
238d