FDA applicant

Bard Interventional Products Div.

Billerica, MA2 decisions1996–19980 recalls

FDA records 2 decisions for Bard Interventional Products Div. (Billerica, MA) from 1996 to 1998: 2 510(k) clearances. All are in product code KNS (Unit, Electrosurgical, Endoscopic (With Or…). Its devices cite 3 predicates, 0 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, gastroenterology and urology panel, where it files most

How often FDA has decided Bard Interventional Products Div.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bard Interventional Products Div. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Bard”

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

Bard Peripheral Vascular, Inc. 46 Bard Access Systems, Inc. 22 Bard Cardiosurgery Div 3 Bard Diagnostic Sciences,Inc. 3 Bard Medical Div. 3 Bard Access Systems, Inc. (C.R. Bard, Inc.) 3 Bard Electrophysiology 3 Bard Access Systems, Inc. (Bard Has Joined Bd) 2 Bard Peripheral Vacular, Inc. 1 Bard Reproductive Systems 1 Bard Gynecology and Radiology 1 Bard Electro Medical Systems, Inc. 1

Bard Interventional Products Div.

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?

Other applicant names beginning “Bard”