GASTROINTESTINAL TUBE— 510(k) K851671

Substantially Equivalent

Sheridan Catheter Corp.

FDA 510(k) clearance K851671 for GASTROINTESTINAL TUBE, Substantially Equivalent on 1985-06-14. Applicant: Sheridan Catheter Corp..

Clearance details

Applicant: Sheridan Catheter Corp.
Product code: Code KNT
Advisory panel: Gastroenterology, Urology
Date received: 1985-04-23
Decision date: 1985-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Argyle, NY, US

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Adverse events under product code KNT

product code KNT

Death: 192
Injury: 6,034
Malfunction: 4,049
Other: 1
Total: 10,276

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.