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 Angioslide, Ltd. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 15, 2017: PROTEUS PTA Balloon Catheter with Embolic Capture Feature.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Dec 15, 2017 | PROTEUS PTA Balloon Catheter with Embolic Capture FeatureK172494 · LIT | 510(k) clearances |
| Dec 6, 2013 | PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATUREK133043 · LIT | 510(k) clearances |
| Jun 8, 2012 | PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATUREK120164 · LIT | 510(k) clearances |
| Apr 13, 2012 | PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATUREK120805 · LIT | 510(k) clearances |
| Jul 21, 2011 | EXTRA PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE; PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATUREK111750 · DQY | 510(k) clearances |
| Mar 23, 2010 | EXTRA PTA BALLOON CATHETER WITH EMBOLIC PROTECTION FEATUREK090364 · LIT | 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
