510(k) Report

FDA applicant

Ronald A. Sherman

Irvine, CA1 decision2004–20040 recalls

FDA records 1 decision for Ronald A. Sherman (Irvine, CA) in 2004: 1 510(k) clearance. All are in product code NQK (Maggots, Medical). No recall is linked to its devices.

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

How often FDA has decided Ronald A. Sherman’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ronald A. Sherman since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ronald A. Sherman 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?

  • NQKMaggots, Medical1decision

Who builds on its devices?

Later devices cite its devices 3 times; 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.

  • K033391Medical MaggotsRonald A. Sherman · 20043cite it

What has FDA decided for it lately?

  • K033391Medical MaggotsRonald A. Sherman · 2004

The one decision as Ronald A. Sherman →

Other applicant names beginning “Ronald”

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

Ronald D. Shippert, M.D. 1