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 American Research Products with 56 510(k) clearances. The most recent is a 510(k) clearance dated Mar 1, 1995: BUN REAGENT.
| Mar 1, 1995 | BUN REAGENTK942984 · CDQ | 510(k) clearances |
| Jul 19, 1990 | BIURET (COLORMETRIC), TOTAL PROTEINK901527 · CEK | 510(k) clearances |
| May 31, 1990 | PHOSPHORUS REAGENTS PROD CODES 7763/7764/7563/7463K901964 · CEO | 510(k) clearances |
| May 31, 1990 | IRON REAGENTS PRODUCT CODES 7725 AND 7726K901960 · JMO | 510(k) clearances |
| May 2, 1990 | COLORIMETRIC CHLORIDE PRODUCT #4314125K900827 · CHI | 510(k) clearances |
| Apr 25, 1990 | NAD REDUCTION, ALT/SPGT CODES 7722,7723,7422,7522K901702 · CKA | 510(k) clearances |
| Apr 19, 1990 | AMRESCO LDH-L REAGENTS PRODUCTS #7710, 7711K900667 · CFJ | 510(k) clearances |
| Apr 19, 1990 | AMRESCO CREATININE REAGENTS PRODUCT #7790, 7791K900666 · CGX | 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
