R.E. Brown Co., Inc. · Class III · Cleared Jul 27, 1978
| K-number | K780781 |
| Device name | STILITH CARDIAC PACEMAKERS-M. 60 & 120 |
| Applicant | R.E. Brown Co., Inc. |
| Product code | DXY |
| Device class | Class III |
| Decision date | Jul 27, 1978 |
| Decision | Substantially Equivalent |
| Regulation | 870.3610 |
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