PAN (CHIBA ASPIRATING NEEDLE)— 510(k) K970872

Name: FDA 510(k) clearance K970872
Creator: U.S. Food and Drug Administration
Published: 1997-05-21

Substantially Equivalent

Gallini Intl., Inc.

FDA 510(k) clearance K970872 for PAN (CHIBA ASPIRATING NEEDLE), Substantially Equivalent on 1997-05-21. Applicant: Gallini Intl., Inc.. Device class: 2.

Clearance details

Applicant: Gallini Intl., Inc.
Product code: Code KNW
Device class: Class 2
Regulation: 21 CFR 876.1075
Advisory panel: Gastroenterology, Urology
Date received: 1997-03-10
Decision date: 1997-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Glen Allen, VA, US

Download summary PDF View on FDA.gov ↗

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K962568 — ACRI ILIAC CREST ASPIRATION BIOPSY NEEDLES1996-11-25

Adverse events under product code KNW

product code KNW

Death: 9
Injury: 965
Malfunction: 10,444
Other: 3
Total: 11,421

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.