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 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Hotspur Technologies with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 24, 2015: 0.018 Arrow GPSCath Balloon Dilatation Catheter (150 cm).
| Jun 24, 2015 | 0.018 Arrow GPSCath Balloon Dilatation Catheter (150 cm)K143093 · LIT | 510(k) clearances |
| Sep 17, 2014 | Arrow GPSCath Balloon Dialation Catheter (150 cm)K142300 · LIT | 510(k) clearances |
| Jul 2, 2014 | ARROW GPSCATH BALLOON DILATATION CATHETERK140351 · LIT | 510(k) clearances |
| Jun 20, 2013 | ARROW GPSCATH BALLOON DILATATION CATHETERK130397 · LIT | 510(k) clearances |
| Jan 20, 2012 | GPSCATH BALLON DILATATION CATHETERK113769 · LIT | 510(k) clearances |
| Jul 13, 2010 | PTA-DUO PTA BALLOON CATHETERK101047 · LIT | 510(k) clearances |
| Jul 12, 2010 | PTA-PLUS PTA BALLOON CATHER 5 MM X 4CM, PTA-PLUS PTA BALLOON CATHETER 6MM X 4CMK100842 · DXE | 510(k) clearances |
| Jul 12, 2010 | EMBO PLUS EMBOLECTOMY CATHETERK100840 · DXE | 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
