FDA applicant

Bard Diagnostic Sciences,Inc.

Redmond, WA3 decisions1997–19980 recalls

FDA records 3 decisions for Bard Diagnostic Sciences,Inc. (Redmond, WA) from 1997 to 1998: 3 510(k) clearances. All are in product code MMW (System, Test, Tumor Marker, Monitoring, Bladder). Its devices cite 2 predicates, 2 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, immunology panel, where it files most

How often FDA has decided Bard Diagnostic Sciences,Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bard Diagnostic Sciences,Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bard Diagnostic Sciences,Inc.’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 “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 Medical Div. 3 Bard Access Systems, Inc. (C.R. Bard, Inc.) 3 Bard Electrophysiology 3 Bard Interventional Products Div. 2 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 Diagnostic Sciences,Inc.

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?

Other applicant names beginning “Bard”