FDA applicant
Kerberos Proximal Solutions, Inc.
FDA records 6 decisions for Kerberos Proximal Solutions, Inc. (Mountain View, CA) from 2003 to 2006: 6 510(k) clearances. Most are in product codes DQO (Catheter, Intravascular, Diagnostic) and QEZ (Aspiration Thrombectomy Catheter). Its devices cite 23 predicates, 5 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Kerberos Proximal Solutions”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Kerberos Proximal Solutions, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Kerberos Proximal Solutions, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Kerberos Proximal Solutions, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report