510(k) Report

FDA applicant

Rapid Mfg. Co.

Atlanta, GA1 decision1999–19990 recalls

FDA records 1 decision for Rapid Mfg. Co. (Atlanta, GA) in 1999: 1 510(k) clearance. All are in product code GXY (Electrode, Cutaneous). 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 Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rapid Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Rapid Mfg. Co. 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?

  • GXYElectrode, Cutaneous1decision

What has FDA decided for it lately?

  • K982096Dermastim Plus, Pigtails, Flexstim Superflex, Flexstim Plus, Carbonstim Vertastim, EnduroRapid Mfg. Co. · 1999

The one decision as Rapid Mfg. Co. →

Other applicant names beginning “Rapid”

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

Rapid Medical, Ltd. 12Rapid City Regional Hospital, Inc. 10Rapid Biomedical GmbH 7Rapid Diagnostic Laboratories, Inc. 6Rapid Diagnostics, Inc. 4Rapid Pathogen Screening, Inc. 3Rapid Aid Corp. 3Rapid Injection Systems Corp. 2Rapid Reboot Recovery Products, LLC 2Rapid-Aid Ltd./Ltee 1Rapid Response Solutions, LLC 1Rapid Nexus Nanotech Wound Solutions, Inc. 1