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 Padpro, LLC with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 28, 2002: PADPRO, MODEL 2502.
| May 28, 2002 | PADPRO, MODEL 2502K020743 · MKJ | 510(k) clearances |
| May 8, 2002 | PADPRO MODEL #2516K020203 · MKJ | 510(k) clearances |
| Feb 27, 2002 | PADPRO, MODEL 2603K020288 · MKJ | 510(k) clearances |
| Jan 18, 2002 | PADPRO MODEL 2001, 2001-S, 2001-C, 2001-EPSK014209 · MKJ | 510(k) clearances |
| Sep 4, 2001 | PADPRO SYSTEM DEFIBRILLATOR ELECTRODE ADAPTERSK003548 · MKJ | 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
