BARD HIGH FLOW PAPILLOTOME— 510(k) K963484

Name: FDA 510(k) clearance K963484
Creator: U.S. Food and Drug Administration
Published: 1996-11-19

Substantially Equivalent

Bard Interventional Products Div.

FDA 510(k) clearance K963484 for BARD HIGH FLOW PAPILLOTOME, Substantially Equivalent on 1996-11-19. Applicant: Bard Interventional Products Div.. Device class: 2.

Clearance details

Applicant: Bard Interventional Products Div.
Product code: Code KNS
Device class: Class 2
Regulation: 21 CFR 876.4300
Advisory panel: Gastroenterology, Urology
Date received: 1996-09-03
Decision date: 1996-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Billerica, MA, US

Download summary PDF View on FDA.gov ↗

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K982557 — BARD PROFORMA AND APOLLO PRE-CURVED PAPILLOTOMES1998-09-10

Adverse events under product code KNS

product code KNS

Death: 44
Injury: 2,361
Malfunction: 4,771
Total: 7,176

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.