Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Pantex with 17 510(k) clearances. The most recent is a 510(k) clearance dated May 8, 2012: PANTEX AM/PM SALIVARY CORTISOL ENZYME IMMUNOASSAY.
| Date | Record | Source |
|---|---|---|
| May 8, 2012 | PANTEX AM/PM SALIVARY CORTISOL ENZYME IMMUNOASSAYK102841 · NHG | 510(k) clearances |
| Feb 24, 1995 | NEOSCREEN ELISA TSHK942658 · JLW | 510(k) clearances |
| Dec 28, 1994 | NEOSCREEN ELISA HYDROXYPROGESTERONEK940233 · JLX | 510(k) clearances |
| Sep 30, 1991 | PROLACTIN IRMA IMMUNOMAGK914107 · CFT | 510(k) clearances |
| Aug 12, 1991 | FSH IRMA IMMUNOMAGK912804 · CGJ | 510(k) clearances |
| Jun 18, 1991 | NEONATAL BLOOD SPOT TEST 17-HYDROXPROG RADIO KITK911839 · JLX | 510(k) clearances |
| Apr 12, 1991 | LH IRMA IMMUNOMAGK911050 · CEP | 510(k) clearances |
| Mar 19, 1991 | PANTEX IRMA LH 1251 KITK910717 · CEP | 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
