CORPAK GASTROSTOMY TUBE — Corpak Co. (510(k) K931921)
CORPAK GASTROSTOMY TUBE — Corpak Co. (510(k) K931921) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: CORPAK GASTROSTOMY TUBE; Applicant: Corpak Co.; Clearance track: 510(k).
| Device name | CORPAK GASTROSTOMY TUBE |
|---|---|
| Applicant | Corpak Co. |
| Clearance track | 510(k) |
| Submission number | K931921 |
| Decision | Substantially Equivalent |
| Decision date | 1995-06-09 |
| Date received | 1993-04-16 |
| Product code | KNT |
| Device class | 2 |
| Medical specialty | Gastroenterology, Urology |
| Applicant location | IL, US |
| Source | openFDA device |
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$1999/mo
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