FDA applicant

Harvard Clinical Technology

South Natick, MA2 decisions2003–20052 recalls

FDA records 2 decisions for Harvard Clinical Technology (South Natick, MA) from 2003 to 2005: 2 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and MEA (Pump, Infusion, Pca). 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Harvard Clinical Technology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Harvard Clinical Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Harvard Clinical Technology’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 “Harvard”

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

Harvard Apparatus, Inc. 9 Harvard Laboratories 8 Harvard Medical Devices, Ltd. 5

Harvard Clinical Technology

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?

What has been recalled?

Other applicant names beginning “Harvard”