Vanguard Biomedical Corp.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ministick Pregnancy Test Ref K960733
Regimes: 510(k) Registry: 510(k)Proclinic One Step Pregnancy Test Ref K914253
Regimes: 510(k) Registry: 510(k)Miniclinic Ovulation Prediction Test Ref K910351
Regimes: 510(k) Registry: 510(k)Miniclinic Ovulation Predictor Ref K960233
Regimes: 510(k) Registry: 510(k)Miniclinic Pregnancy Test Ref K894012
Regimes: 510(k) Registry: 510(k)Proclinic One-Step Dipstick Pregnancy Test Ref K930014
Regimes: 510(k) Registry: 510(k)Homeclinic One Step Pregnancy Test Ref K914254
Regimes: 510(k) Registry: 510(k)Home Clinic Pregnancy Test Ref K883826
Regimes: 510(k) Registry: 510(k)Miniclinic Ovulation Prediction Test Ref K891762
Regimes: 510(k) Registry: 510(k)Modified Homeclinic Pregnancy Test Ref K895560
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vanguard Biomedical Corp. have in the registry?
The registry currently lists 10 devices for Vanguard Biomedical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vanguard Biomedical Corp.'s devices?
Among its 10 most recently registered devices, Vanguard Biomedical Corp. has devices listed in FDA 510(k) (10 devices).
What risk classes do Vanguard Biomedical Corp.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Vanguard Biomedical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vanguard Biomedical Corp. in the registry?
The most recently registered devices listed for Vanguard Biomedical Corp. include MINISTICK PREGNANCY TEST, PROCLINIC ONE STEP PREGNANCY TEST, MINICLINIC OVULATION PREDICTION TEST and MINICLINIC OVULATION PREDICTOR.