ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT— 510(k) K102274

Name: FDA 510(k) clearance K102274
Creator: U.S. Food and Drug Administration
Published: 2011-06-15

Substantially Equivalent

Arvik Enterprises/ Mini Lap Technologies

FDA 510(k) clearance K102274 for ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENT, Substantially Equivalent on 2011-06-15. Applicant: Arvik Enterprises/ Mini Lap Technologies. Device class: 1.

Clearance details

Applicant: Arvik Enterprises/ Mini Lap Technologies
Product code: Code GAA
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 2010-08-11
Decision date: 2011-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shelton, CT, 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.