Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Schiapparelli Biosystems, Inc. with 24 510(k) clearances. The most recent is a 510(k) clearance dated Jul 13, 1999: ACE LDL-C REAGENT, LDL-C CALIBRATOR, LDL-C CONTROLS.
| Jul 13, 1999 | ACE LDL-C REAGENT, LDL-C CALIBRATOR, LDL-C CONTROLSK991733 · MRR | 510(k) clearances |
| Jun 10, 1998 | ACE T UPTAKE REAGENT TU CALIBRATORSK981375 · KHQ | 510(k) clearances |
| Jun 10, 1998 | ACE T4 REAGENT T4 CALIBRATORSK981377 · KLI | 510(k) clearances |
| Nov 12, 1997 | ACE VALPROIC ACID REAGENT, AED CALIBRATORSK973581 · LEG | 510(k) clearances |
| Nov 12, 1997 | ACE PRIMIDONE REAGENT, AED CALIBRATORSK973582 · DJD | 510(k) clearances |
| Nov 12, 1997 | ACE THEOPHYLLINE REAGENT, THEO CALIBRATORSK973583 · KLS | 510(k) clearances |
| Nov 6, 1997 | ACE PHENOBARBITAL REAGENT/AED CALIBRATORSK973536 · DLJ | 510(k) clearances |
| Nov 4, 1997 | ACE PHENYTOIN REAGENT, AED CALIBRATORSK973414 · DIP | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
