Armkel, LLC · Class I · Cleared Oct 3, 1995
| K-number | K953581 |
| Device name | FIRST RESPONSE OVULATION PREDICTOR TEST |
| Applicant | Armkel, LLC |
| Product code | CEP |
| Device class | Class I |
| Decision date | Oct 3, 1995 |
| Decision | Substantially Equivalent |
| Regulation | 862.1485 |
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