Em Diagnostic Systems, Inc. · Class II · Cleared Aug 17, 1990
| K-number | K903333 |
| Device name | CREATINE KINASE TEST (CK) ITEM NUMBER 65411 |
| Applicant | Em Diagnostic Systems, Inc. |
| Product code | CGS |
| Device class | Class II |
| Decision date | Aug 17, 1990 |
| 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