INSTAFLO BOWEL CATHETER SYSTEM KIT— 510(k) K100273

Unknown

Hollister, Inc.

FDA 510(k) clearance K100273 for INSTAFLO BOWEL CATHETER SYSTEM KIT, Unknown on 2010-04-22. Applicant: Hollister, Inc..

Clearance details

Applicant: Hollister, Inc.
Product code: Code KNT
Advisory panel: Gastroenterology, Urology
Date received: 2010-01-29
Decision date: 2010-04-22
Decision: Unknown
Clearance type: Special
Location: Libertyville, IL, 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.