| K-number | K760886 |
| Device name | RECTAL TUBE DEVICE |
| Applicant | Van Sickle Plastics Co. |
| Product code | EXB |
| Device class | Class I |
| Decision date | Dec 9, 1976 |
| Decision | Substantially Equivalent |
| Regulation | 876.5900 |
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