Taidoc Technology Corporation · Class II · Cleared Oct 4, 2011
| K-number | K103487 |
| Device name | FORA PNC100 DIGITAL PREGANCY TEST, TD-5301 PREGANCY TEST |
| Applicant | Taidoc Technology Corporation |
| Product code | LCX |
| Device class | Class II |
| Decision date | Oct 4, 2011 |
| 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