FDA applicant

Pace Tech, Inc.

Clearwater, FL18 decisions1988–19960 recalls

FDA records 18 decisions for Pace Tech, Inc. (Clearwater, FL) from 1988 to 1996: 18 510(k) clearances. Most are in product codes DQA (Oximeter) and MHX (Monitor, Physiological, Patient (With…). 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 Tech, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pace Tech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pace Tech, 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 “Pace”

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

Pace Medical 20 Pace Tech Medical Monitors, Inc. 3 Pace Surgical 3 Pace Pharmaceutical Services, Inc. 2 Pace West 1

Pace Tech, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pace”