Seppim S.A.S. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Seppim S.A.S. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Seppim S.A.S. has 6 FDA 510(k) cleared medical devices. Based in Bothell, US.
Historical record: 6 cleared submissions from 2010 to 2011. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Seppim S.A.S. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Seppim S.A.S.
6 devices
Cleared
Nov 18, 2011
ELITECH CLINICAL SYSTEMS CREATINNE PAP SL MODEL CRSL-0250, CLITECH CLINICAL...
Chemistry
366d
Cleared
May 19, 2011
ELITECH CLINICAL SYSTEMS HBA1C REAGENT, ELITECH CLINCAL SYSTEM HBA1C...
Chemistry
448d
Cleared
May 19, 2011
ELITECH CLINICAL SYSTEMS TRIGLYCERIDES SL, ELITECH CLINICAL SYSTEMS...
Chemistry
223d
Cleared
May 06, 2011
ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTS
Chemistry
463d
Cleared
Dec 15, 2010
ELITECH CLINICAL SYSTEMS GLUCOSE PAP SL ELITECH CLINICAL SYSTEMS ELICAL 2,...
Chemistry
294d
Cleared
Sep 20, 2010
AST/GOT 4+1 SL, AST/GOT 4+1 SL, ELICAL 2, ELITROL I, ELITROL II, MODEL...
Chemistry
276d