Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Kerberos Proximal Solutions with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 20, 2006: RINSPIRATION CATHETER SYSTEM, MODELS 50135, 550135, P7065, P70135.
| Sep 20, 2006 | RINSPIRATION CATHETER SYSTEM, MODELS 50135, 550135, P7065, P70135K062275 · QEZ | 510(k) clearances |
| May 13, 2005 | KERBEROS PROXIMAL SOLUTIONS RISPIRATION SYSTEMK050130 · QEZ | 510(k) clearances |
| Aug 26, 2004 | RINSPIRATION SYSTEM,RINSPIRATION SYSTEM SHORT TIP, MODELS FG01477/FG01703K041123 · DQO | 510(k) clearances |
| Jul 22, 2004 | KERBEROS OCCLUDING GUIDE CATHETER AND ACCESSORIESK041151 · DQY | 510(k) clearances |
| May 21, 2004 | RINSPIRATION SYSTEMK041291 · DQO | 510(k) clearances |
| Sep 25, 2003 | RINSPIRATION SYSTEMK031485 · DQO | 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
