Philips Healthcare (Suzhou) Co., Lit.
ChinaFDA applicant, unverified
- Devices
- 1
What Philips Healthcare (Suzhou) Co., Lit. makes
Philips Healthcare (Suzhou) Co., Ltd. manufactures the DigitalDiagnost C50, a diagnostic imaging device designed for medical imaging applications.
The DigitalDiagnost C50 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
DigitalDiagnost C50 Ref K201725
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Philips Healthcare (Suzhou) Co., Lit. have in the registry?
The registry currently lists 1 device for Philips Healthcare (Suzhou) Co., Lit.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Philips Healthcare (Suzhou) Co., Lit.'s devices?
Among its 1 most recently registered device, Philips Healthcare (Suzhou) Co., Lit. has devices listed in FDA 510(k) (1 device).
What risk classes do Philips Healthcare (Suzhou) Co., Lit.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Philips Healthcare (Suzhou) Co., Lit.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Philips Healthcare (Suzhou) Co., Lit. in the registry?
The most recently registered devices listed for Philips Healthcare (Suzhou) Co., Lit. include DigitalDiagnost C50.