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 13, 2026, FDA's public records list Z-Kat, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 24, 2003: Z-BOX.
| Date | Record | Source |
|---|---|---|
| Apr 24, 2003 | Z-BOXK030764 · HAW | 510(k) clearances |
| Dec 20, 2002 | VOYAGER LINUXK023975 · HAW | 510(k) clearances |
| Oct 3, 2001 | MODIFICATION TO FLOUROLAB PLUSK013025 · HAW | 510(k) clearances |
| Dec 4, 2000 | FLUOROLAB PLUSK002893 · HAW | 510(k) clearances |
| Jun 23, 1999 | Z KAT FLUROTACTIC GUIDANCE SYSTEM MKIK984298 · HAW | 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
