Medscand AB
SwedenFDA applicant, unverified
- Devices
- 2
What Medscand AB makes
Medscand AB manufactures disposable plastic vaginal specula, including the Easy-Spec model 303, and the Accellon Cervical Biosampler, a device designed for cervical biosampling.
These products are classified as Class II medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Medscand Disposable Plastic Vaginal Speculum; Easy-Spec Plastic Vaginal Speculum, Model 303 Ref K984211
Regimes: 510(k) Registry: 510(k)Accellon Cervical Biosampler Ref K911432
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medscand AB have in the registry?
The registry currently lists 2 devices for Medscand AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medscand AB's devices?
Among its 2 most recently registered devices, Medscand AB has devices listed in FDA 510(k) (2 devices).
What risk classes do Medscand AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medscand AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medscand AB in the registry?
The most recently registered devices listed for Medscand AB include MEDSCAND DISPOSABLE PLASTIC VAGINAL SPECULUM; EASY-SPEC PLASTIC VAGINAL SPECULUM, MODEL 303 and ACCELLON CERVICAL BIOSAMPLER.