JACKSON FINE NEEDLE ASPIRATION SYSTEM— 510(k) K896606

Name: FDA 510(k) clearance K896606
Creator: U.S. Food and Drug Administration
Published: 1990-01-04

Substantially Equivalent

National-Standard Medical Products

FDA 510(k) clearance K896606 for JACKSON FINE NEEDLE ASPIRATION SYSTEM, Substantially Equivalent on 1990-01-04. Applicant: National-Standard Medical Products. Device class: 1.

Clearance details

Applicant: National-Standard Medical Products
Product code: Code GAA
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1989-11-21
Decision date: 1990-01-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gainesville, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GAA

product code GAA

Malfunction: 834
Total: 834

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.