FDA applicant

Micro Interventional Systems, Inc.

Sunnyvale, CA1 decision1995–19950 recalls

FDA records 1 decision for Micro Interventional Systems, Inc. (Sunnyvale, CA) in 1995: 1 510(k) clearance. All are in product code DQT (Occluder, Catheter Tip). 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 Micro Interventional Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micro Interventional Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Micro Interventional Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?