This page includes the latest FDA filings for Shenzhen Qianhai Huolilang Technology Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3016725120 |
| FEI Number | 3016725120 |
| Name | N/A |
| Owner & Operator | Shenzhen Qianhai Huolilang Technology Co., Ltd. |
| Contact Address | Room 201, Building A, No. 1 Qianwan 1st shenzhen CN-44 Guangdong 518052 CN |
| Official Correspondent |
|
| US Agent | |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | N/A N/A N/A, NA N/A US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
N/A [Shenzhen Qianhai Huolilang Technology Co., Ltd.] | MASK HLL01 | 2020-03-15 |