| K-number | K892117 |
| Device name | GENTLEHALER(R) |
| Applicant | Schering Research |
| Product code | CCQ |
| Device class | Class I |
| Decision date | Jun 23, 1989 |
| Decision | Substantially Equivalent |
| Regulation | 868.5640 |
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