Diagnostics 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 14, 2026, FDA's public records list Pan Probe Biotech with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jul 15, 2002: LIVESURE HCG URINARY PREGNANCY TEST STRIP AND TEST CARD.
| Jul 15, 2002 | LIVESURE HCG URINARY PREGNANCY TEST STRIP AND TEST CARDK020968 · JHI | 510(k) clearances |
| Nov 26, 2001 | LIVESURE METHADONE SCREEN TESTSK013796 · DJR | 510(k) clearances |
| Jul 20, 2001 | LIVESURE BARBITURATES SCREEN TESTK012133 · DIS | 510(k) clearances |
| Jul 20, 2001 | LIVESURE BENZODIAZEPINES SCREEN TESTSK012131 · JXM | 510(k) clearances |
| Jul 20, 2001 | LIVESURE PHENECYCLINE (PCP) SCREEN TESTSK012107 · LCM | 510(k) clearances |
| Jun 8, 2001 | LIVESURE AMPHETAMINE SCREEN TESTK011609 · DKZ | 510(k) clearances |
| Jun 8, 2001 | LIVESURE METHAMPHETAMINE SCREEN TESTSK011610 · LAF | 510(k) clearances |
| Apr 17, 2001 | LIVESURE COCAINE SCREEN TESTK010967 · DIO | 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
