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 15, 2026, FDA's public records list Navarre Biomedical Ltd. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Nov 7, 1996: NAVARRE PERCUTANEOUS BILIARY DRAINAGE.
| Nov 7, 1996 | NAVARRE PERCUTANEOUS BILIARY DRAINAGEK955110 · FGE | 510(k) clearances |
| Feb 7, 1996 | OPTI-DRAIN MULTI-USE DRAINAGE CATHETERK955505 · GBX | 510(k) clearances |
| Jun 2, 1995 | NAVARRE N-FUSER(TM) PERIPHERAL INFUSION CATHETERK945909 · KRA | 510(k) clearances |
| May 15, 1995 | NAVARRE LOCKING PIGTAIL UNIVERSAL DRAINAGE CATHETERK951907 · GBX | 510(k) clearances |
| Apr 24, 1995 | NAVARRE UNIVERSAL DRAINAGE CATHETERK951475 · GBX | 510(k) clearances |
| Sep 8, 1994 | NAVARRE 600 ML DRAINAGE BAGK943663 · EXF | 510(k) clearances |
| Jul 8, 1994 | NAVARRE PERCUTANEOUS ACCESS SETK942315 · KGZ | 510(k) clearances |
| Mar 28, 1994 | NAVARRE BIOMEDICAL TIP-LOCKING DRAINAGE CATHETERSK933600 · GBX | 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
