FDA applicant

Vidco, Inc.

Beaverton, OR7 decisions1989–19971 recall

FDA records 7 decisions for Vidco, Inc. (Beaverton, OR) from 1989 to 1997: 7 510(k) clearances. Most are in product codes DXJ (Display, Cathode-Ray Tube, Medical) and DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). Its devices cite 5 predicates, 5 of them its own earlier devices. 1 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, cardiovascular panel, where it files most

How often FDA has decided Vidco, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vidco, Inc. since 2007.

Recalls per year

1in 2015

2007high 1 (2015) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Vidco, 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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Vidco, Inc.

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?