Dr. F. Ross Sharp, Ltd.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Dr. F. Ross Sharp, Ltd. makes
Dr. F. Ross Sharp, Ltd. manufactures the INVIRO Syringe, a pre-filled syringe designed for precise medication delivery in clinical settings.
The INVIRO Syringe is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Inviro Syringe Ref K941450
510(k) 510(k)
Frequently asked questions
How many devices does Dr. F. Ross Sharp, Ltd. have in the registry?
The registry currently lists 1 device for Dr. F. Ross Sharp, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. F. Ross Sharp, Ltd.'s devices?
Among its 1 most recently registered device, Dr. F. Ross Sharp, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dr. F. Ross Sharp, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dr. F. Ross Sharp, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dr. F. Ross Sharp, Ltd. in the registry?
The most recently registered devices listed for Dr. F. Ross Sharp, Ltd. include INVIRO SYRINGE.