N-Dia, Inc. · Class I · Cleared Feb 2, 2004
| K-number | K030849 |
| Device name | AMNISURE FETAL MEMBRANES RUPTURE TEST MODEL FMRT1 |
| Applicant | N-Dia, Inc. |
| Product code | JJX |
| Device class | Class I |
| Decision date | Feb 2, 2004 |
| Decision | Substantially Equivalent |
| Regulation | 862.1660 |
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