Gould, Inc. · Class II · Cleared Jul 22, 1991
| K-number | K911935 |
| Device name | CARDIAC ELECTROPHYSICAL LEAD SELECTOR, MODIFIED |
| Applicant | Gould, Inc. |
| Product code | DRR |
| Device class | Class II |
| Decision date | Jul 22, 1991 |
| Decision | Substantially Equivalent |
| Regulation | 870.2050 |
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