| K-number | K901501 |
| Device name | CORPAK GASTROSTOMY TUBE |
| Applicant | Corpak Co. |
| Product code | KGC |
| Device class | Class II |
| Decision date | Jun 11, 1990 |
| Decision | Substantially Equivalent |
| Regulation | 876.5980 |
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