510(k) Report

FDA applicant

Advanced Video Products, Inc.

Washington, DC3 decisions1986–19950 recalls

FDA records 3 decisions for Advanced Video Products, Inc. (Washington, DC) from 1986 to 1995: 3 510(k) clearances. 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 Advanced Video Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Video Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Advanced Video Products, 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