Harbin Quanke Medi-Technical Development Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3005280264
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Harbin Quanke Medi-Technical Development Co., Ltd. makes
Harbin Quanke Medi-Technical Development Co., Ltd. manufactures the QK-Systemic Therapeutic Apparatus, a device designed for systemic therapeutic interventions.
The QK-Systemic Therapeutic Apparatus is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway in the United States.
Catalogue
Qk-Systemic Therapeutic Apparatus Ref K141892
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3005280264
- Address
- 42-1 LANE 2, JING WEI STREET, HARBIN Heilongjiang
Frequently asked questions
How many devices does Harbin Quanke Medi-Technical Development Co., Ltd. have in the registry?
The registry currently lists 1 device for Harbin Quanke Medi-Technical Development Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Harbin Quanke Medi-Technical Development Co., Ltd.'s devices?
Among its 1 most recently registered device, Harbin Quanke Medi-Technical Development Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Harbin Quanke Medi-Technical Development Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Harbin Quanke Medi-Technical Development Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Harbin Quanke Medi-Technical Development Co., Ltd. in the registry?
The most recently registered devices listed for Harbin Quanke Medi-Technical Development Co., Ltd. include QK-SYSTEMIC THERAPEUTIC APPARATUS.