FDA applicant

Pulse Life, Inc.

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Pulse Life, Inc. (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code BWK (Stimulator, Electro-Acupuncture). No recall is linked to its devices.

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

How often FDA has decided Pulse Life, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pulse Life, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pulse Life, 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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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 Time Products, Ltd. 6 Pulse Metric, Inc. 5 Pulse Biomedical, Inc. 3 Pulse Scientific, Inc. 3 Pulse Medical Instruments 1 Pulse Med, Inc. 1

Pulse Life, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Pulse”