Medical device makerLabelled 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 American Laboratory Products Co. with 27 510(k) clearances. The most recent is a 510(k) clearance dated Jan 29, 2002: CIC-C1Q EIA.
| Jan 29, 2002 | CIC-C1Q EIAK012576 · DAK | 510(k) clearances |
| May 30, 2001 | ALPCO MILENIA ANTI-TG EIAK011415 · JZO | 510(k) clearances |
| May 24, 2001 | ALPCO MILENIA ANTI-TPO ELISAK011201 · JZO | 510(k) clearances |
| Feb 17, 1998 | ORGENTEC ANTI-MPO (P-ANCA) ELISAK974701 · MOB | 510(k) clearances |
| Feb 17, 1998 | ORGENTEC ANTI-PR3 (C-ANCA) ELISAK974702 · MOB | 510(k) clearances |
| Jul 14, 1997 | THYROGLOBULIN ASSAY SYSTEMK972190 · JZO | 510(k) clearances |
| Apr 8, 1997 | ORGENTEC MICRO-ALBUMIN EIA ASSAYK970932 · JIR | 510(k) clearances |
| Nov 18, 1996 | ORGENTEC ANTI-SM ELISAK962062 · LJM | 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
