Delaware Prosthetics, Inc. · Class I · Cleared Dec 19, 1983
| K-number | K832151 |
| Device name | PDM SILOXANE PROSTHETIC ORBIT |
| Applicant | Delaware Prosthetics, Inc. |
| Product code | GBI |
| Device class | Class I |
| Decision date | Dec 19, 1983 |
| Decision | Substantially Equivalent |
| Regulation | 878.3800 |
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