CORPAK GASTROSTOMY TUBE— 510(k) K901501

Substantially Equivalent

Corpak Co.

FDA 510(k) clearance K901501 for CORPAK GASTROSTOMY TUBE, Substantially Equivalent on 1990-06-11. Applicant: Corpak Co..

Clearance details

Applicant: Corpak Co.
Product code: Code KGC
Advisory panel: Gastroenterology, Urology
Date received: 1990-03-30
Decision date: 1990-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheeling, IL, US

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Adverse events under product code KGC

product code KGC

Death: 7
Total: 7

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.