| K-number | K941584 |
| Device name | CREATINE KINASE METHOD |
| Applicant | Dupont Medical Products |
| Product code | JHS |
| Device class | Class II |
| Decision date | Jul 6, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 862.1215 |
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