ENTEROCLYSIS TUBE— 510(k) K923002

Unknown

Biosearch Medical Products, Inc.

FDA 510(k) clearance K923002 for ENTEROCLYSIS TUBE, Unknown on 1994-06-28. Applicant: Biosearch Medical Products, Inc..

Clearance details

Applicant: Biosearch Medical Products, Inc.
Product code: Code KNT
Advisory panel: Gastroenterology, Urology
Date received: 1992-06-22
Decision date: 1994-06-28
Decision: Unknown
Clearance type: Traditional
Location: Somerville, NJ, US

Download summary PDF View on FDA.gov ↗

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.