FDA applicant

Pace Tech Medical Monitors, Inc.

Clearwater, FL3 decisions1993–19980 recalls

FDA records 3 decisions for Pace Tech Medical Monitors, Inc. (Clearwater, FL) from 1993 to 1998: 3 510(k) clearances. Most are in product codes BXN (Stimulator, Nerve, Battery-Powered) and DQA (Oximeter). 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 Medical Monitors, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pace Tech Medical Monitors, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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 Surgical 3 Pace Pharmaceutical Services, Inc. 2 Pace West 1

Pace Tech Medical Monitors, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pace”