L.T.C. PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE— 510(k) K897181

Unknown

Intl. Medical Marketing, Inc.

FDA 510(k) clearance K897181 for L.T.C. PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE, Unknown on 1990-03-27. Applicant: Intl. Medical Marketing, Inc..

Clearance details

Applicant: Intl. Medical Marketing, Inc.
Product code: Code FPD
Advisory panel: Gastroenterology, Urology
Date received: 1989-12-28
Decision date: 1990-03-27
Decision: Unknown
Clearance type: Traditional
Location: Ridge, NY, US

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Adverse events under product code FPD

product code FPD

Death: 6
Other: 1
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.