510(k) Report

FDA applicant

Rapid Machine & Tool Corp.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Rapid Machine & Tool Corp. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code HAW (Neurological Stereotaxic Instrument). 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, neurology panel, where it files most

How often FDA has decided Rapid Machine & Tool Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rapid Machine & Tool Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Rapid”

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