FDA applicant

Victor

Washington, DC1 decision1986–19860 recalls

FDA records 1 decision for Victor (Washington, DC) in 1986: 1 510(k) clearance. All are in product code CAN (Regulator, Pressure, Gas Cylinder). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Victor since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Victor”

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

Victor Medical Instruments Co., Ltd. 1 Victor Co. of Japan, Ltd. C/O Jvc Corp. 1 Victor John Manley 1

Victor

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Victor”