510(k) Report

FDA applicant

Scott Imaging Intl., Inc.

Mobile, AL7 decisions1994–19950 recalls

FDA records 7 decisions for Scott Imaging Intl., Inc. (Mobile, AL) from 1994 to 1995: 7 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and IZO (Generator, High-Voltage, X-Ray, Diagnostic). 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 Scott Imaging Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Scott Imaging Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Scott”

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