Tylenol Medical Instruments Co., Ltd.
ChinaFDA 510(k) applicant, unverified FDA FEI 3013513837
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Tylenol Medical Instruments Co., Ltd. makes
Tylenol Medical Instruments Co., Ltd. makes CO2 sampling lines.
The company's devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
CO2 Sampling Line Ref K181981
510(k) 510(k)
Company details
- FDA FEI number
- 3013513837
- Address
- 3rd Floor, No.10, Xinhua Road, Sanjiao Town,, Zhongshan Guangdong
Frequently asked questions
How many devices does Tylenol Medical Instruments Co., Ltd. have in the registry?
The registry currently lists 1 device for Tylenol Medical Instruments Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tylenol Medical Instruments Co., Ltd.'s devices?
Among its 1 most recently registered device, Tylenol Medical Instruments Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Tylenol Medical Instruments Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tylenol Medical Instruments Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tylenol Medical Instruments Co., Ltd. in the registry?
The most recently registered devices listed for Tylenol Medical Instruments Co., Ltd. include CO2 Sampling Line.