| K-number | K801330 |
| Device name | ANSPACH LEG SUPPORT |
| Applicant | The Anspach Effort, Inc. |
| Product code | CCX |
| Device class | Class I |
| Decision date | Jun 26, 1980 |
| Decision | Substantially Equivalent |
| Regulation | 868.6820 |
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