| K-number | K802829 |
| Device name | SCANLAN VASCU-STATT |
| Applicant | Scanlan Intl., Inc. |
| Product code | FMP |
| Device class | Class I |
| Decision date | Jan 15, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 880.6450 |
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