Medical Diagnostic Technologies, Inc. · Class I · Cleared Oct 25, 1988
| K-number | K883083 |
| Device name | MYCOPLASMA PNEUMONIAE ANTIBODY LATEX TEST SYSTEM |
| Applicant | Medical Diagnostic Technologies, Inc. |
| Product code | GSA |
| Device class | Class I |
| Decision date | Oct 25, 1988 |
| Decision | Substantially Equivalent |
| Regulation | 866.3375 |
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