FDA applicant

Intersect Systems, Inc.

Longview, WA21 decisions1983–20021 recall

FDA records 21 decisions for Intersect Systems, Inc. (Longview, WA) from 1983 to 2002: 21 510(k) clearances. Most are in product codes CIG (Diazo Colorimetry, Bilirubin) and DPS (Electrocardiograph). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

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

Recalls per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

Class I Class II/III not classified

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

Planning a device like Intersect Systems, 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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Other applicant names beginning “Intersect”

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

Intersect Medical Products, Inc. 5 Intersect Ent. 2

Intersect Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Intersect”