Diagnostic Products Corp. · Class I · Cleared Apr 10, 1997
| K-number | K971051 |
| Device name | IMMULITE THYROID AUTOANTIBODY CONTROL MODULE |
| Applicant | Diagnostic Products Corp. |
| Product code | JJX |
| Device class | Class I |
| Decision date | Apr 10, 1997 |
| 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