FDA applicant

Pulse Time Products, Ltd.

Chichester, W. Sussex, GB6 decisions1981–19900 recalls

FDA records 6 decisions for Pulse Time Products, Ltd. (Chichester, W. Sussex, GB) from 1981 to 1990: 6 510(k) clearances. Most are in product codes DRT (Monitor, Cardiac (Incl. Cardiotachometer &…) and DXN (System, Measurement, Blood-Pressure…). 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 Pulse Time Products, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pulse Time Products, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pulse Time Products, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Pulse”

FDA records each applicant name separately; these may or may not be the same firm.

Pulse Biosciences, Inc. 7 Pulse Metric, Inc. 5 Pulse Biomedical, Inc. 3 Pulse Scientific, Inc. 3 Pulse Medical Instruments 1 Pulse Life, Inc. 1 Pulse Med, Inc. 1

Pulse Time Products, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pulse”