| K-number | K920143 |
| Device name | TB SUSCEPTIBILITY QUADS I AND II |
| Applicant | Remel Co. |
| Product code | MJD |
| Device class | Class II |
| Decision date | Jun 9, 1992 |
| Decision | Substantially Equivalent |
| Regulation | 866.1700 |
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