LAKE GASTROSTOMY TUBE— 510(k) K902121

Substantially Equivalent

Lake Medical Products, Inc.

FDA 510(k) clearance K902121 for LAKE GASTROSTOMY TUBE, Substantially Equivalent on 1990-07-27. Applicant: Lake Medical Products, Inc..

Clearance details

Applicant: Lake Medical Products, Inc.
Product code: Code KGC
Advisory panel: Gastroenterology, Urology
Date received: 1990-05-11
Decision date: 1990-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

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.