Terumo Medical Corp. · Class II · Cleared May 22, 1984
| K-number | K841601 |
| Device name | TERUMO SENSIBEAD THYROXINE EIA KIT |
| Applicant | Terumo Medical Corp. |
| Product code | KLI |
| Device class | Class II |
| Decision date | May 22, 1984 |
| Decision | Substantially Equivalent |
| Regulation | 862.1700 |
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