FDA applicant

Traverse Medical Monitors

Saline, MI2 decisions1987–19880 recalls

FDA records 2 decisions for Traverse Medical Monitors (Saline, MI) from 1987 to 1988: 2 510(k) clearances. Most are in product codes CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase) and CBS (Analyzer, Gas, Halothane, Gaseous-Phase…). 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, anesthesiology panel, where it files most

How often FDA has decided Traverse Medical Monitors’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Traverse Medical Monitors since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Traverse Medical Monitors’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 “Traverse”

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

Traverse Vascular, Inc. 1

Traverse Medical Monitors

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Traverse”