FDA applicant

Micor, Inc.

Allison Park, PA8 decisions1986–20030 recalls

FDA records 8 decisions for Micor, Inc. (Allison Park, PA) from 1986 to 2003: 8 510(k) clearances. Most are in product codes BSO (Catheter, Conduction, Anesthetic) and DQY (Catheter, Percutaneous). Its devices cite 6 predicates, 3 of them its own earlier devices. 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 Micor, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micor, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Micor, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Micor, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?