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 Atomic Products with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jan 17, 1992: SPECT TABLE, MODEL #056-760.
| Date | Record | Source |
|---|---|---|
| Jan 17, 1992 | SPECT TABLE, MODEL #056-760K915541 · IYZ | 510(k) clearances |
| Sep 6, 1991 | THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900K913055 · IZD | 510(k) clearances |
| Nov 29, 1990 | ECONOMY C-ARM TABLE, MODEL # 056-005K904187 · IXQ | 510(k) clearances |
| Nov 6, 1990 | RADIOGRAPHIC TRANSPORT, TRAUMA MODEL 056-230, 235K904623 · IXQ | 510(k) clearances |
| May 11, 1990 | DIGITAL IMAGE ENHANCEMENT SYSTEMK900851 · LLZ | 510(k) clearances |
| Feb 1, 1990 | RECTILINEAR SCANNER MODEL #187-270K895799 · IYW | 510(k) clearances |
| Feb 16, 1989 | ATOMLAB 100, MODEL 086-250 & 200 MODEL 086-270K884312 · KPT | 510(k) clearances |
| Apr 11, 1988 | VENTI-SCAN IIK871868 · IYT | 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
