FDA applicant

Intersect Medical Products, Inc.

Walker, MI5 decisions1979–19940 recalls

FDA records 5 decisions for Intersect Medical Products, Inc. (Walker, MI) from 1979 to 1994: 5 510(k) clearances. Most are in product codes CAP (Monitor, Airway Pressure (Includes Gauge…) and CAH (Filter, Bacterial, Breathing-Circuit). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Intersect Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Systems, Inc. 21 Intersect Ent. 2

Intersect Medical Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Intersect”