Schiapparelli Biosystems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Schiapparelli Biosystems, Inc. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Schiapparelli Biosystems, Inc. has 24 FDA 510(k) cleared chemistry devices. Based in Fairfield, US.
Historical record: 24 cleared submissions from 1993 to 1999.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Schiapparelli Biosystems, Inc.
24 devices
Cleared
Jul 13, 1999
ACE LDL-C REAGENT, LDL-C CALIBRATOR, LDL-C CONTROLS
Chemistry
53d
Cleared
Jun 10, 1998
ACE T UPTAKE REAGENT TU CALIBRATORS
Chemistry
55d
Cleared
Jun 10, 1998
ACE T4 REAGENT T4 CALIBRATORS
Chemistry
55d
Cleared
Nov 12, 1997
ACE VALPROIC ACID REAGENT, AED CALIBRATORS
Toxicology
51d
Cleared
Nov 12, 1997
ACE PRIMIDONE REAGENT, AED CALIBRATORS
Toxicology
51d
Cleared
Nov 12, 1997
ACE THEOPHYLLINE REAGENT, THEO CALIBRATORS
Toxicology
51d
Cleared
Nov 06, 1997
ACE PHENOBARBITAL REAGENT/AED CALIBRATORS
Chemistry
49d
Cleared
Nov 04, 1997
ACE PHENYTOIN REAGENT, AED CALIBRATORS
Toxicology
56d
Cleared
Oct 20, 1997
ACE CARBAMAZEPINE REAGENT/AED CALIBRATORS
Chemistry
32d
Cleared
May 21, 1997
ACE HDL-C REAGENT
Chemistry
23d
Cleared
Dec 11, 1995
HDL PRECIPITATING REAGENT
Chemistry
96d
Cleared
Oct 23, 1995
TRIGLYCERIDES REAGENT
Chemistry
47d