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 Bioclinical Systems with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jun 30, 1995: CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIA.
| Jun 30, 1995 | CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIAK950196 · JTY | 510(k) clearances |
| Apr 4, 1995 | CULTURE MEDIA, ANTIMICROBIAL SUSCEPTIBILITY TEST, MUELLER HINTON AGARSK945911 · JTZ | 510(k) clearances |
| Feb 9, 1994 | MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGARK933122 · JTY | 510(k) clearances |
| Feb 3, 1994 | MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGARK933121 · JTY | 510(k) clearances |
| Aug 24, 1987 | ROUND 1K873086 · JXA | 510(k) clearances |
| Apr 21, 1986 | MICRO-ELISA HLH TEST KIT MONOCLONALK860333 · CEP | 510(k) clearances |
| Apr 21, 1986 | VISI-CHECK HLH TEST MONOCLONALK860334 · CEP | 510(k) clearances |
| Apr 11, 1986 | MICRO-EIA THEOPHYLLINE TEST KIT MONOCLONALK855227 · KLS | 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
