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 15, 2026, FDA's public records list Meloy Laboratories, Inc. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Jun 21, 1985: SS-A(RO) & SS-B(LA) ANTIBODY ASSAY.
| Jun 21, 1985 | SS-A(RO) & SS-B(LA) ANTIBODY ASSAYK852033 · DHN | 510(k) clearances |
| Jan 4, 1985 | MELOY LAB-ANTINUCLEAR ANTIBODY TEST-HEP-2 CELL CULK844678 · DHN | 510(k) clearances |
| Jul 19, 1984 | MELOY IMMUNOSTAT MONOCLONAL FACTOR VIIIK841708 · GGP | 510(k) clearances |
| Jun 26, 1984 | MELOY AUTOANTIBODY TEST SYSK842247 · DBM | 510(k) clearances |
| Jul 18, 1983 | ANTI-ENA TESTK831292 · LKO | 510(k) clearances |
| Feb 12, 1982 | ANA TEST (MOUSE LIVER SUBSTRATE)K820265 · DHN | 510(k) clearances |
| Jan 22, 1982 | TOTAL HEMOLYTIC COMPLEMENT TEST KITK820005 · | 510(k) clearances |
| May 15, 1981 | HUMAN IGG-ALBUMIN TEST KITK811178 · CJQ | 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
