510(k) Report

FDA applicant

Bd/Preefil

Franklin Lakes, NJ1 decision2000–20000 recalls

FDA records 1 decision for Bd/Preefil (Franklin Lakes, NJ) in 2000: 1 510(k) clearance. All are in product code FOZ (Catheter, Intravascular, Therapeutic…). Its devices cite 1 predicate, 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, general hospital panel, where it files most

How often FDA has decided Bd/Preefil’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bd/Preefil since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

  • Bd2citations

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K982558BD Preefile Normal Saline Flush Syringe Flush SyringeBd/Preefil · 20002cite it

What has FDA decided for it lately?

  • K982558BD Preefile Normal Saline Flush Syringe Flush SyringeBd/Preefil · 2000

The one decision as Bd/Preefil →