510(k) Report

FDA applicant

Igc-Medical Advances, Inc.

Milwaukee, WI7 decisions2000–20040 recalls

FDA records 7 decisions for Igc-Medical Advances, Inc. (Milwaukee, WI) from 2000 to 2004: 7 510(k) clearances. All are in product code MOS (Coil, Magnetic Resonance, Specialty). 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 Igc-Medical Advances, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Igc-Medical Advances, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Igc-Medical Advances, 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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