510(k) Report

FDA applicant

Imnet Systems, Inc.

Alpharetta, GA1 decision1997–19970 recalls

FDA records 1 decision for Imnet Systems, Inc. (Alpharetta, GA) in 1997: 1 510(k) clearance. All are in product code LMD (System, Digital Image Communications…). 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 Imnet Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Imnet Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Imnet Systems, 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