510(k) Report

FDA applicant

Rapid Aid Corp.

Mississauga, CA3 decisions2004–20170 recalls

FDA records 3 decisions for Rapid Aid Corp. (Mississauga, CA) from 2004 to 2017: 3 510(k) clearances. Most are in product codes MPO (Infant Heel Warmer (Chemical Heat Pack)) and IMD (Pack, Hot Or Cold, Disposable). Its devices cite 5 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Rapid Aid , Ltd.”.

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

FIG. A — Illustration, physical medicine panel, where it files most

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

FDA decisions per year

1in 2017

2015: 12017: 1
2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Rapid Aid Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Rapid”

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