Devices and Diagnostics Consulting Group · Class I · Cleared Dec 22, 1998
| K-number | K972788 |
| Device name | CROSSLAPS ELISA |
| Applicant | Devices and Diagnostics Consulting Group |
| Product code | JMM |
| Device class | Class I |
| Decision date | Dec 22, 1998 |
| Decision | Substantially Equivalent |
| Regulation | 862.1400 |
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