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 Pace Tech with 18 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 1996: VITALMAX 4000/MINIPACK 3100/3000.
| Date | Record | Source |
|---|---|---|
| Nov 21, 1996 | VITALMAX 4000/MINIPACK 3100/3000K951226 · DSK | 510(k) clearances |
| Jul 1, 1996 | VITALMAX 4100K953795 · CBS | 510(k) clearances |
| Feb 22, 1995 | HANDYPACK 911SCK944541 · CCK | 510(k) clearances |
| Jan 31, 1995 | VITALMAX 800 PLUS/VITALMAX 810 PLUS/MINIPACK 300K945385 · MHX | 510(k) clearances |
| Aug 11, 1994 | MINIPACK 911-STCK925701 · CCK | 510(k) clearances |
| Aug 10, 1994 | MINIPACK 3100/3000 MODIFICATIONK934385 · DXN | 510(k) clearances |
| Jul 19, 1994 | VITALMAX 4000K933624 · MHX | 510(k) clearances |
| Sep 3, 1993 | VITALMAX 800-CK930559 · CCK | 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
