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 Bio-Analytics Laboratories with 19 510(k) clearances. The most recent is a 510(k) clearance dated May 29, 1986: KINETIC ALKALINE PHOSPHATASE REAGENT KIT.
| May 29, 1986 | KINETIC ALKALINE PHOSPHATASE REAGENT KITK861638 · CJE | 510(k) clearances |
| Mar 14, 1986 | ENZYMATIC ALPHA-AMYLASE REAGENT KITK860245 · JFJ | 510(k) clearances |
| Feb 11, 1986 | ALBUMIN REAGENT KITK860213 · CIX | 510(k) clearances |
| May 20, 1985 | ULTRA-VIOLET GLUCOSE REAGENTK851514 · CFA | 510(k) clearances |
| May 20, 1985 | ULTRA-VIOLET BUN REAGENT KITK851513 · CDQ | 510(k) clearances |
| Mar 5, 1985 | ENZYMATIC ALPHA-AMYLASE REAGENT KITK850639 · CIW | 510(k) clearances |
| Oct 28, 1983 | ERYTHROCYTE TESTK832771 · LKZ | 510(k) clearances |
| Sep 12, 1983 | ACETAMINOPHEN(PARACETAMOLK832567 · LDP | 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
