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 14, 2026, FDA's public records list Western Laboratories Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 11, 1984: HEPARINOMETER.
| Jun 11, 1984 | HEPARINOMETERK834024 · KFF | 510(k) clearances |
| Apr 12, 1983 | MODEL 200K830468 · FTZ | 510(k) clearances |
| Jul 2, 1982 | MODEL 100 BICARBONATE CONDUCTIVITYK821834 · FKQ | 510(k) clearances |
| May 27, 1982 | MODEL 80 BCK821414 · | 510(k) clearances |
| May 27, 1982 | MODEL 90 BCK821415 · FLB | 510(k) clearances |
| Jul 28, 1980 | MODEL 90 PRESSURE/CONDUCTIVITY/TEMP TESTK801303 · KDI | 510(k) clearances |
| Aug 31, 1978 | MODEL 80 CONDUCTIVITY/TEMP.TEST UNITK780932 · FIZ | 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
