Advocacy International, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advocacy International, Ltd. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Advocacy International, Ltd. has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1981 to 1988.
Browse the FDA 510(k) cleared devices submitted by Advocacy International, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Advocacy International, Ltd.
13 devices
Cleared
May 27, 1988
LIPASE UV [TOYO]
Chemistry
238d
Cleared
Jan 19, 1988
SEPACELL R-500 AND SEPACELL R-500A
General Hospital
124d
Cleared
Feb 04, 1986
MODIFICATION ASAHI NEW PAN-SERIES HEMOFILTERS
Gastroenterology & Urology
36d
Cleared
Jan 21, 1986
ASAHI AM SERIES DIALYZERS
Gastroenterology & Urology
22d
Cleared
Jan 08, 1986
SEPACELL R-500 & SEPACELL R-500A
General Hospital
77d
Cleared
Aug 12, 1984
TOYO JOZO URIC ACID TEST
Chemistry
79d
Cleared
Aug 10, 1984
TOYO JOZO G-GTP TEST
Chemistry
77d
Cleared
Mar 17, 1983
ASAHI HOLLOW FIBER KIDNEYS NR SERIES
Gastroenterology & Urology
58d
Cleared
Mar 17, 1983
ASAHI HOLLOW FIBER KIDNEYS, AM-SERIES
Gastroenterology & Urology
58d
Cleared
Jan 14, 1983
EIKEN KIZAI ARTIFICIAL KIDNEY BLOOD CIR
Gastroenterology & Urology
32d
Cleared
Dec 14, 1981
FLOWGUARD CATHETERS & CANNALAE
Cardiovascular
47d
Cleared
Nov 27, 1981
POLYSTAN HEART LUNG MACHINE SYS
Cardiovascular
30d
Cleared
Nov 27, 1981
POLYSTAN VERTICLUDE BLOOD PUMP
Cardiovascular
30d