FDA applicant

Merrimack Laboratories

Hudson, MA6 decisions1980–19850 recalls

FDA records 6 decisions for Merrimack Laboratories (Hudson, MA) from 1980 to 1985: 6 510(k) clearances. Most are in product codes HHR (Laser, Surgical, Gynecologic) and EOQ (Bronchoscope (Flexible Or Rigid)). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Merrimack Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Merrimack Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Merrimack Laboratories

Which product codes does it file in?

What has FDA decided for it lately?