510(k) Report

FDA applicant

James K. Brannon

Culver City, CA2 decisions1996–19960 recalls

FDA records 2 decisions for James K. Brannon (Culver City, CA) in 1996: 2 510(k) clearances. All are in product code FMF (Syringe, Piston). 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 James K. Brannon’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for James K. Brannon since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — James K. Brannon 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?

  • FMFSyringe, Piston2decisions

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K960049Brannon PortsyringeJames K. Brannon · 19961cites it

What has FDA decided for it lately?

  • K960049Brannon PortsyringeJames K. Brannon · 1996
  • K960047Brannon Pedi PortsyringeJames K. Brannon · 1996

All 2 as James K. Brannon →

Other applicant names beginning “James”

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

James River Corp. 15James L. Geraci & Associates, Inc. 5James Leckey Design 2James J. Schramm 1James R. Powell 1James Nguyen 1James D Rusin MD, MBA 1James P Boyd 1James Consolidated, Inc. 1James J. Lally 1James Alexander Corp. 1James Korea Co., Ltd. 1