510(k) Report

FDA applicant

Cumes-Honikman Partnership

Santa Barbara, CA1 decision1987–19870 recalls

FDA records 1 decision for Cumes-Honikman Partnership (Santa Barbara, CA) in 1987: 1 510(k) clearance. All are in product code FFD (Evacuator, Bladder, Manually Operated). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Cumes-Honikman Partnership’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cumes-Honikman Partnership since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cumes-Honikman Partnership by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FFDEvacuator, Bladder, Manually Operated1decision

What has FDA decided for it lately?

  • K874410CumevacCumes-Honikman Partnership · 1987

The one decision as Cumes-Honikman Partnership →