PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH.— 510(k) K901791

Name: FDA 510(k) clearance K901791
Creator: U.S. Food and Drug Administration
Published: 1990-08-08

Unknown

Southside Biotechnology

FDA 510(k) clearance K901791 for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING CATH., Unknown on 1990-08-08. Applicant: Southside Biotechnology. Device class: 2.

Clearance details

Applicant: Southside Biotechnology
Product code: Code KGC
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1990-04-19
Decision date: 1990-08-08
Decision: Unknown
Clearance type: Traditional
Location: Willoughby Hills, OH, US

Download summary PDF View on FDA.gov ↗

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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.