InsufflatOR Needle— 510(k) K142700

Substantially Equivalent

Gynetech Pty. , Ltd.

FDA 510(k) clearance K142700 for InsufflatOR Needle, Substantially Equivalent on 2014-12-19. Applicant: Gynetech Pty. , Ltd..

Clearance details

Applicant: Gynetech Pty. , Ltd.
Product code: Code HIF
Advisory panel: Obstetrics/Gynecology
Date received: 2014-09-22
Decision date: 2014-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Thomastown, AU

Download summary PDF View on FDA.gov ↗

Adverse events under product code HIF

product code HIF

Death: 19
Injury: 578
Malfunction: 5,639
Total: 6,236

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.