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 13, 2026, FDA's public records list Ampcor, Inc. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Jul 14, 1992: INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TEST.
| Date | Record | Source |
|---|---|---|
| Jul 14, 1992 | INFECTIOUS MONONUCLEOSIS QIK-DOT IM DRY CARD TESTK922297 · KTN | 510(k) clearances |
| Jul 14, 1992 | IMFECTIOUS MONONUCLEOSIS IM LIQUID CARD TESTK922296 · KTN | 510(k) clearances |
| Sep 13, 1991 | DIPSTICK SALMONELLAK910438 · GRM | 510(k) clearances |
| Aug 21, 1989 | SINGLE AND DUAL BAND DIPSTICK HCG TESTK893873 · DHA | 510(k) clearances |
| Jun 9, 1989 | QUIK-DOT TOXOPLASMOSISK890048 · LLA | 510(k) clearances |
| Apr 14, 1989 | C REACTIVE PROTEIN LIQUIDK892146 · DCK | 510(k) clearances |
| Apr 14, 1989 | QUIK-DOT C REACTIVE PROTEINK892119 · DCK | 510(k) clearances |
| Jan 31, 1989 | QUIK-DOT ANTISTREPTOLYSIN-OK890025 · GTQ | 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
