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 14, 2026, FDA's public records list Sicel Technologies, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 13, 2008: DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM.
| Nov 13, 2008 | DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEMK083035 · NZT | 510(k) clearances |
| Aug 4, 2008 | MODIFICATION TO ONEDOSE PATIENT DOSIMETRY SYSTEMK081859 · IYE | 510(k) clearances |
| Jan 23, 2008 | DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEMK080004 · NZT | 510(k) clearances |
| Jun 20, 2007 | DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODEL DVS-I-11: DVS INSERTION TOOL, DVS-D-A: DVS DOSIMETER, DVS-R-100K071399 · LHN | 510(k) clearances |
| Jun 13, 2006 | DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODELS DVS-I-11, DVS INSERTION TOOL, DVS-D-A, DVS DOSIMETERK061051 · LHN | 510(k) clearances |
| Apr 3, 2006 | DOSE VERIFICATION SYSTEMK052118 · LHN | 510(k) clearances |
| Jun 25, 2004 | ONEDOSE PATIENT DOSIMETRY SYSTEMK040687 · IYE | 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
