Langfang Huilong Plastic Product Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 2
What Langfang Huilong Plastic Product Co., Ltd. makes
Langfang Huilong Plastic Product Co., Ltd. makes powder-free vinyl patient examination gloves and powdered vinyl patient examination gloves.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Powder-Free Vinyl Patient Examination Gloves Ref K071685
Regimes: 510(k) Registry: 510(k)Powdered Vinyl Patient Examination Gloves Ref K071686
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Langfang Huilong Plastic Product Co., Ltd. have in the registry?
The registry currently lists 2 devices for Langfang Huilong Plastic Product Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Langfang Huilong Plastic Product Co., Ltd.'s devices?
Among its 2 most recently registered devices, Langfang Huilong Plastic Product Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Langfang Huilong Plastic Product Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Langfang Huilong Plastic Product Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Langfang Huilong Plastic Product Co., Ltd. in the registry?
The most recently registered devices listed for Langfang Huilong Plastic Product Co., Ltd. include POWDER-FREE VINYL PATIENT EXAMINATION GLOVES and POWDERED VINYL PATIENT EXAMINATION GLOVES.