FDA applicant

Reeves Manufactoring

Frederick, MD1 decision1994–19940 recalls

FDA records 1 decision for Reeves Manufactoring (Frederick, MD) in 1994: 1 510(k) clearance. All are in product code BTM (Ventilator, Emergency, Manual (Resuscitator)). 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 Reeves Manufactoring’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Reeves Manufactoring since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Reeves”

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

Reeves Scientific, Inc. 1

Reeves Manufactoring

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Reeves”