510(k) Report

FDA applicant

Pulseflow Technologies

Aylesbury, GB1 decision2015–20150 recalls

FDA records 1 decision for Pulseflow Technologies (Aylesbury, GB) in 2015: 1 510(k) clearance. All are in product code JOW (Sleeve, Limb, Compressible). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

How often FDA has decided Pulseflow Technologies’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015: 1
2015high 1 (2015) · low 0 (2016)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — Pulseflow Technologies by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • JOWSleeve, Limb, Compressible1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K150806PulseFlowDFPulseflow Technologies · 2015

The one decision as Pulseflow Technologies →