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 SSCOR with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 18, 2004: S-SCORT...JR QUICKDRAW, MODEL 2400.
| Date | Record | Source |
|---|---|---|
| May 18, 2004 | S-SCORT...JR QUICKDRAW, MODEL 2400K041154 · BTA | 510(k) clearances |
| Mar 5, 1997 | S-SCORT (2500)K964997 · BTA | 510(k) clearances |
| Jun 16, 1995 | S-SCORTK952632 · BTA | 510(k) clearances |
| Apr 25, 1995 | SSCOR/BOARD ..3 MODEL 23000 PRE-ASSEMBLED SUCTION SYSTEM FOR PATIENT TRANSPORT VEHICLESK950464 · GCX | 510(k) clearances |
| Dec 22, 1994 | S-SCORT(R)DUET MODEL 2014 PORTABLE SUCTION PUMPK945929 · BTA | 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
