| K-number | K802421 |
| Device name | UCG-BETA STAT |
| Applicant | Armkel, LLC |
| Product code | JHJ |
| Device class | Class II |
| Decision date | Oct 23, 1980 |
| 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