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 14, 2026, FDA's public records list Pro-Tec Containers with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 14, 1994: PRO-TEC DISPOSABLE SHARPS CONTAINERS IR180 & IR80.
| Dec 14, 1994 | PRO-TEC DISPOSABLE SHARPS CONTAINERS IR180 & IR80K945274 · FMI | 510(k) clearances |
| Dec 14, 1994 | PRO-TEC DISPOSBLE SHARPS CONTAINERS Q1K945275 · FMI | 510(k) clearances |
| Dec 14, 1994 | PRO-TEC DISPOSABLE SHARPS CONTAINERS 5GK945276 · FMI | 510(k) clearances |
| Dec 14, 1994 | PRO-TECH DISPOSABLE SHARPS CONTAINERS VNC2K945273 · FMI | 510(k) clearances |
| Dec 2, 1994 | PRO-TEC DISPOSABLE SHARPS CONTAINERSK942179 · FMI | 510(k) clearances |
| Oct 4, 1989 | PRO-JECT(TM) SAFETY NEEDLE HOLDERK892665 · JKA | 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
