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 Protos Laboratories with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 31, 1980: GOAT ANTI-HUMAN IGM.
| Date | Record | Source |
|---|---|---|
| Oct 31, 1980 | GOAT ANTI-HUMAN IGMK802177 · DFT | 510(k) clearances |
| Oct 31, 1980 | GOAT ANTI-HUMAN IGG GAMMA CHAIN SPECIFICK802257 · DEW | 510(k) clearances |
| Oct 31, 1980 | GOAT ANTI-HUMAN COMPLEMENT C4K802196 · DBI | 510(k) clearances |
| Sep 24, 1979 | GOAT ANTI-HUMAN C-REACTIVE PROTEINK791560 · DCK | 510(k) clearances |
| Sep 4, 1979 | GOAT ANTI-HUMAN ALPHA-1-ANTITRYPSINK791605 · DEM | 510(k) clearances |
| Aug 3, 1979 | GOAR ANTI-HUMAN LAMBODA CHAINK791115 · DEH | 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
