| K-number | K802205 |
| Device name | ECG/RESPIRATION STIMULATOR |
| Applicant | Healthdyne, Inc. |
| Product code | BZQ |
| Device class | Class II |
| Decision date | Oct 3, 1980 |
| Decision | Substantially Equivalent |
| Regulation | 868.2375 |
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