| K-number | K781843 |
| Device name | RECORDER, HOLTER ELECTROCARDIOGRAM |
| Applicant | Hovik Corp. |
| Product code | DSH |
| Device class | Class II |
| Decision date | Nov 3, 1978 |
| Decision | Substantially Equivalent |
| Regulation | 870.2800 |
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