The following data is part of a premarket notification filed by Guangzhou Wondfo Biotech Co., Ltd. with the FDA for Wondfo Multi-drug Urine Test Cup, Panel.
Device ID | K133968 |
510k Number | K133968 |
Device Name: | WONDFO MULTI-DRUG URINE TEST CUP, PANEL |
Classification | Enzyme Immunoassay, Amphetamine |
Applicant | Guangzhou Wondfo Biotech Co., Ltd. 504 EAST DIAMOND AVE. SUITE F Gaithersburg, MD 20878 |
Contact | Joe Shia |
Correspondent | Joe Shia Guangzhou Wondfo Biotech Co., Ltd. 504 EAST DIAMOND AVE. SUITE F Gaithersburg, MD 20878 |
Product Code | DKZ |
CFR Regulation Number | 862.3100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-12-26 |
Decision Date | 2014-02-25 |
Summary: | summary |