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 15, 2026, FDA's public records list Nordiclab International with 8 510(k) clearances. The most recent is a 510(k) clearance dated Sep 26, 1980: NORDICLAB PROSTATIC ACID PHOSPHATASE RIA.
| Sep 26, 1980 | NORDICLAB PROSTATIC ACID PHOSPHATASE RIAK801988 · JFH | 510(k) clearances |
| Sep 16, 1980 | NORDICLAB FERRITIN IRMA TESTK801989 · DBF | 510(k) clearances |
| May 14, 1980 | NORDICLAB TESTOSTERONE RIA TESTK800921 · CDZ | 510(k) clearances |
| May 14, 1980 | NORDICLAB PROGESTERONE RIA TESTK800922 · JLS | 510(k) clearances |
| May 14, 1980 | NORDICLAB ESTRADIOL RIA TESTK800920 · CHP | 510(k) clearances |
| Nov 13, 1979 | NORDICLAB TOTAL ESTRIOL RIA TESTK792189 · CGI | 510(k) clearances |
| Jan 17, 1979 | IRMA TEST, NORDICLAB FERRITINK782157 · JMG | 510(k) clearances |
| Jan 10, 1979 | RIA TEST, NORDICALB HPLK782099 · JMF | 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
