Washington Regulatory Services
Country not established
- Devices
- 3
What Washington Regulatory Services makes
Washington Regulatory Services manufactures diagnostic and procedural devices, including an angioscope for pulmonary artery visualization, intra-uterine and intra-folopian transfer systems, and disposable hysterography cupulas for imaging.
These products are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company operates within the United States.
Catalogue
Angioscope For Pulmonary Artery Use Ref K882658
Regimes: 510(k) Registry: 510(k)Intra-Uterine Transfer, Intra-Folopian Transfer Ref K983604
Regimes: 510(k) Registry: 510(k)Register, A Disposable Hysterography Cupula Ref K894259
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Washington Regulatory Services have in the registry?
The registry currently lists 3 devices for Washington Regulatory Services. Devices recorded under merged duplicate company entries are counted once.
Which registries list Washington Regulatory Services's devices?
Among its 3 most recently registered devices, Washington Regulatory Services has devices listed in FDA 510(k) (3 devices).
What risk classes do Washington Regulatory Services's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Washington Regulatory Services's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Washington Regulatory Services in the registry?
The most recently registered devices listed for Washington Regulatory Services include ANGIOSCOPE FOR PULMONARY ARTERY USE, INTRA-UTERINE TRANSFER, INTRA-FOLOPIAN TRANSFER and REGISTER, A DISPOSABLE HYSTEROGRAPHY CUPULA.