| K-number | K791844 |
| Device name | CRITIFLO & CRITIFLO DOME |
| Applicant | Gould, Inc. |
| Product code | KRA |
| Device class | Class II |
| Decision date | Oct 2, 1979 |
| Decision | Substantially Equivalent |
| Regulation | 870.1210 |
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