510(k) Report

FDA applicant

Rapid-Aid Ltd./Ltee

Mississuaga,Ontario, CA1 decision1996–19960 recalls

FDA records 1 decision for Rapid-Aid Ltd./Ltee (Mississuaga,Ontario, CA) in 1996: 1 510(k) clearance. All are in product code ITX (Transducer, Ultrasonic, Diagnostic). 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, radiology panel, where it files most

How often FDA has decided Rapid-Aid Ltd./Ltee’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rapid-Aid Ltd./Ltee since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Which product codes does it file in?

  • ITXTransducer, Ultrasonic, Diagnostic1decision

What has FDA decided for it lately?

  • K963169Rapid-Aid Therapeutic/Scanning Ultrasound GelRapid-Aid Ltd./Ltee · 1996

The one decision as Rapid-Aid Ltd./Ltee →

Other applicant names beginning “Rapid-Aid”

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 Mfg. Co. 1Rapid Response Solutions, LLC 1Rapid Nexus Nanotech Wound Solutions, Inc. 1