Bayer Corp. · Class II · Cleared Jul 22, 1999
| K-number | K991817 |
| Device name | ADDITIONAL IMS ASSAYS FOR THE BAYER ADVIA IMS SYSTEM |
| Applicant | Bayer Corp. |
| Product code | CIJ |
| Device class | Class II |
| Decision date | Jul 22, 1999 |
| Decision | Substantially Equivalent |
| Regulation | 862.1070 |
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