Worldwide Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 9
What Worldwide Medical Corp. makes
Worldwide Medical Corp. manufactures home drug test panels and individual tests, including the First Check Home Drug Test Panel 2, Panel 3, Panel 4, and specific tests for MDMA (ecstasy) and THC.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Balloon Thermodilution Catheters Ref K894401
Regimes: 510(k) Registry: 510(k)First Check Home Drug Test Panel 3 Ref K994138
Regimes: 510(k) Registry: 510(k)First Check Home Drug Test Panel 4 Ref K993852
Regimes: 510(k) Registry: 510(k)Polycath #wmc-900 Ref K912270
Regimes: 510(k) Registry: 510(k)First Check Home Drug Test Panel 2 Ref K994139
Regimes: 510(k) Registry: 510(k)First Check Home Drug Test For Mdma (Ecstasy) Ref K020869
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
First Check Home Drug Test (Thc) Ref K993663
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Worldwide Medical Corp. have in the registry?
The registry currently lists 9 devices for Worldwide Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Worldwide Medical Corp.'s devices?
Among its 9 most recently registered devices, Worldwide Medical Corp. has devices listed in FDA 510(k) (9 devices).
What risk classes do Worldwide Medical Corp.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Worldwide Medical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Worldwide Medical Corp. in the registry?
The most recently registered devices listed for Worldwide Medical Corp. include BALLOON THERMODILUTION CATHETERS, FIRST CHECK HOME DRUG TEST PANEL 3, FIRST CHECK HOME DRUG TEST PANEL 4 and POLYCATH #WMC-900.