| K-number | K965150 |
| Device name | A.C.T. IV |
| Applicant | Remel Co. |
| Product code | JSM |
| Device class | Class I |
| Decision date | Jan 22, 1997 |
| Decision | Substantially Equivalent |
| Regulation | — |
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