FDA applicant

Pace West

Fairfield, CA1 decision1989–19890 recalls

FDA records 1 decision for Pace West (Fairfield, CA) in 1989: 1 510(k) clearance. All are in product code LDD (Dc-Defibrillator, Low-Energy, (Including…). 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 Pace West’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pace West since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pace”

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

Pace Medical 20 Pace Tech, Inc. 18 Pace Tech Medical Monitors, Inc. 3 Pace Surgical 3 Pace Pharmaceutical Services, Inc. 2

Pace West

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pace”