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 Isolab, Inc. with 44 510(k) clearances. The most recent is a 510(k) clearance dated Oct 18, 1996: ISOLAB'S T4 TEST KIT.
| Date | Record | Source |
|---|---|---|
| Oct 18, 1996 | ISOLAB'S T4 TEST KITK951014 · KLI | 510(k) clearances |
| Feb 1, 1996 | NEONATAL CHEMISTRY SYSTEM, GALACTOSE TEST KITK950481 · JIA | 510(k) clearances |
| Jan 26, 1996 | PHENYLALANINE TEST KITK943547 · JNB | 510(k) clearances |
| Sep 21, 1995 | ISOLAB'S GALACTOSE-1-PHOSPHATE URIDYL TRANFERASE TEST KITS 800, 4000 SAMPLEK950803 · JJT | 510(k) clearances |
| Sep 5, 1995 | FLUOROSCAN NEONATALK950415 · KHO | 510(k) clearances |
| Jan 20, 1995 | QUIK-SEP QUANTITATIVE HEMOGLOBIN S ASSAYK942276 · GIQ | 510(k) clearances |
| Jan 20, 1995 | QUIK-SEP QUANTITIVE HEMOGLOBIN S CONTROLSK942222 · JCM | 510(k) clearances |
| Nov 17, 1994 | ISOSCANK944185 · JQT | 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
