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 14, 2026, FDA's public records list Spectrum X-Ray with 9 510(k) clearances. The most recent is a 510(k) clearance dated Oct 7, 1993: SPECTRUM DG-P7000 PEDIATRIC CRADLE.
| Oct 7, 1993 | SPECTRUM DG-P7000 PEDIATRIC CRADLEK933134 · KXH | 510(k) clearances |
| Aug 23, 1993 | SPECTRUM MARK I SPECIAL PROCEDURES TABLEK931563 · IXR | 510(k) clearances |
| May 14, 1987 | PENTAMAX 1 MODEL B TABLE SYSTEMK870707 · IXR | 510(k) clearances |
| Feb 21, 1984 | DIGITAL CRADLEK840463 · KXH | 510(k) clearances |
| Feb 21, 1984 | SPECTRUM X-RAY CORPK834494 · IZZ | 510(k) clearances |
| May 19, 1982 | SIMPLAMATIC IIIK827450 · | 510(k) clearances |
| Jan 29, 1982 | SPECTRUM PEDIATRIC CARDLE TABLEK813561 · KXH | 510(k) clearances |
| Nov 5, 1979 | SPECTRUM EMERGENCY & TRAUMA TABLE SYSTEMK791812 · IXR | 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
