Monoclonal Antibodies, Inc. · Class I · Cleared Jul 2, 1986
| K-number | K860924 |
| Device name | RAMP PROGESTURINE PDG ASSAY--48 TEST KIT |
| Applicant | Monoclonal Antibodies, Inc. |
| Product code | JLS |
| Device class | Class I |
| Decision date | Jul 2, 1986 |
| Decision | Substantially Equivalent |
| Regulation | 862.1620 |
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