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 Kemble Instruments with 9 510(k) clearances. The most recent is a 510(k) clearance dated Aug 27, 1984: KEMBLE 405.
| Date | Record | Source |
|---|---|---|
| Aug 27, 1984 | KEMBLE 405K842894 · JQW | 510(k) clearances |
| Oct 14, 1983 | RIA SOFTWAREK832760 · JQP | 510(k) clearances |
| Oct 14, 1983 | KEMTEK 400 RIA GAMMA COUNTERK832734 · JJJ | 510(k) clearances |
| Sep 29, 1983 | KEMTEK 103 RIA GAMMA COUNTERK832735 · JJJ | 510(k) clearances |
| Sep 29, 1983 | KEMTEK 104 RIA GAMMA COUNTERK832736 · JJJ | 510(k) clearances |
| Apr 6, 1983 | KEMTEK 102K830751 · JJJ | 510(k) clearances |
| Aug 24, 1982 | IMMU-COUNT 404K822293 · JJJ | 510(k) clearances |
| Aug 16, 1982 | THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBEK827748 · | 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
