510(k) Report

FDA applicant

Kerberos Proximal Solutions, Inc.

Mountain View, CA6 decisions2003–20060 recalls

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, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

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.

FIG. 1 — Kerberos Proximal Solutions, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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