Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 LKB Instruments with 52 510(k) clearances. The most recent is a 510(k) clearance dated Nov 4, 1987: 1205 BETAPLATE LIQUID SCINTILLATION COUNTER.
| Date | Record | Source |
|---|---|---|
| Nov 4, 1987 | 1205 BETAPLATE LIQUID SCINTILLATION COUNTERK874094 · JJJ | 510(k) clearances |
| Aug 21, 1987 | DELFIA(TM) FERRITIN KITK872955 · JMG | 510(k) clearances |
| Jun 17, 1987 | DELFIA(TM) THYROXINE (T4) KITK871303 · CDX | 510(k) clearances |
| Jun 12, 1987 | DELFIA(TM) HIGE KITK871599 · DHB | 510(k) clearances |
| May 12, 1987 | DELFIA (TM) HTSH KITK871644 · JLW | 510(k) clearances |
| Feb 2, 1987 | DELFIA(TM) TRIIODOTHYRONINE (T3) KITK864452 · CDP | 510(k) clearances |
| Jan 5, 1987 | LKB 2260 MACROTOMEK864733 · IDO | 510(k) clearances |
| Dec 18, 1986 | LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110K862848 · GWC | 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
