Hoffmann-La Roche, Inc. · Class II · Cleared Mar 8, 1982
| K-number | K820391 |
| Device name | ABUSCREEN RADIOIMMUNOASSAY FOR CANNABI |
| Applicant | Hoffmann-La Roche, Inc. |
| Product code | LAT |
| Device class | Class II |
| Decision date | Mar 8, 1982 |
| Decision | Substantially Equivalent |
| Regulation | 862.3870 |
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