Guangzhou Wondfo Biotech Co., Ltd. · Class II · Cleared Apr 21, 2009
| K-number | K072500 |
| Device name | ONE STEP HCG URINE/SERUM TEST |
| Applicant | Guangzhou Wondfo Biotech Co., Ltd. |
| Product code | DHA |
| Device class | Class II |
| Decision date | Apr 21, 2009 |
| Decision | Substantially Equivalent |
| Regulation | 862.1155 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov