FDA applicant

The Mason Clinic

Seattle, WA1 decision1987–19870 recalls

FDA records 1 decision for The Mason Clinic (Seattle, WA) in 1987: 1 510(k) clearance. All are in product code JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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, radiology panel, where it files most

How often FDA has decided The Mason Clinic’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Mason Clinic since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “The”

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

Mason-Keller Corp. 4

The Mason Clinic

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”