510(k) Report

FDA applicant

Interventional Medical, Inc.

Walker, MI4 decisions1982–19880 recalls

FDA records 4 decisions for Interventional Medical, Inc. (Walker, MI) from 1982 to 1988: 4 510(k) clearances. Most are in product codes DQO (Catheter, Intravascular, Diagnostic) and DQX (Wire, Guide, Catheter). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Interventional Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Interventional Medical, 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 “Interventional”

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