| K-number | K800191 |
| Device name | PERITONE |
| Applicant | Laurie Ann Kaiser, Ph.D. |
| Product code | HIR |
| Device class | Class II |
| Decision date | Apr 16, 1980 |
| Decision | Substantially Equivalent |
| Regulation | 884.1425 |
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