FDA applicant

Interventional Therapeutics Corp.

South San Francisco, CA28 decisions1987–19960 recalls

FDA records 28 decisions for Interventional Therapeutics Corp. (South San Francisco, CA) from 1987 to 1996: 28 510(k) clearances. Most are in product codes HCG (Device, Neurovascular Embolization) and DQO (Catheter, Intravascular, Diagnostic). 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 Therapeutics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Interventional Therapeutics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Interventional Therapeutics Corp.’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 “Interventional”

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

Interventional Spine, Inc. 8 Interventional Medical, Inc. 4 Interventional Innovations Corp. 2 Interventional Concepts, Inc. 1 Interventional Research Technologies 1 Interventional Thermodynamics, Inc. 1

Interventional Therapeutics Corp.

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 “Interventional”