Rapid-Aid Ltd./Ltee
CanadaFDA applicant, unverified
- Devices
- 1
What Rapid-Aid Ltd./Ltee makes
Rapid-Aid Ltd./Ltee manufactures therapeutic and scanning ultrasound gel, designed to enhance imaging clarity and patient comfort during ultrasound procedures.
The company’s ultrasound gel is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Rapid-Aid Therapeutic/Scanning Ultrasound Gel Ref K963169
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rapid-Aid Ltd./Ltee have in the registry?
The registry currently lists 1 device for Rapid-Aid Ltd./Ltee. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rapid-Aid Ltd./Ltee's devices?
Among its 1 most recently registered device, Rapid-Aid Ltd./Ltee has devices listed in FDA 510(k) (1 device).
What risk classes do Rapid-Aid Ltd./Ltee's devices fall under?
Among its 1 most recently registered device, the classes recorded for Rapid-Aid Ltd./Ltee's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rapid-Aid Ltd./Ltee in the registry?
The most recently registered devices listed for Rapid-Aid Ltd./Ltee include RAPID-AID THERAPEUTIC/SCANNING ULTRASOUND GEL.