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 Pcl-Ria, Inc. with 29 510(k) clearances. The most recent is a 510(k) clearance dated Apr 5, 1983: B-GCG SYSTEM BY RIA.
| Apr 5, 1983 | B-GCG SYSTEM BY RIAK830526 · JHI | 510(k) clearances |
| Nov 1, 1982 | DIGOXIN KITK823014 · DPB | 510(k) clearances |
| Nov 1, 1982 | THYROID STIMULATING HORMONEK822935 · JLW | 510(k) clearances |
| Sep 30, 1982 | T3 UPTAKE KITSK822612 · KHQ | 510(k) clearances |
| Apr 16, 1982 | THYROXINE T4 KITK820886 · CDX | 510(k) clearances |
| Mar 26, 1982 | FOLLICLE STIMULATING HORMONE KITK820358 · CGJ | 510(k) clearances |
| Mar 25, 1982 | LUTEINIZING HORMONE KITK820357 · CEP | 510(k) clearances |
| Oct 2, 1981 | THYROXINE (T4) 125IK812666 · CDP | 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
