Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Source Production and Equipment Co., Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Nov 4, 2016: Source Production & Equipment Co., Inc. Model M14 192Iridium Brachytherapy Source.
| Nov 4, 2016 | Source Production & Equipment Co., Inc. Model M14 192Iridium Brachytherapy SourceK162573 · KXK | 510(k) clearances |
| Aug 17, 2016 | SPEC Model M23K161396 · KXK | 510(k) clearances |
| Jul 6, 2016 | SPEC Model M13K161395 · KXK | 510(k) clearances |
| Jun 19, 2015 | SPEC Model M16K150895 · KXK | 510(k) clearances |
| Jan 2, 2014 | SPEC MODEL M15K132969 · KXK | 510(k) clearances |
| Apr 22, 2009 | SPEC MODEL M-31K090366 · KXK | 510(k) clearances |
| Apr 19, 2006 | SOURCE PRODUCTION & EQUIPMENT CO, INC., MODEL M-19 IR-192 BRACHYTHERAPY SOURCEK052947 · JAQ | 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
