AP 50/30 Insufflator with Insuflow Port— 510(k) K170799

Substantially Equivalent

Lexion Medical, LLC

FDA 510(k) clearance K170799 for AP 50/30 Insufflator with Insuflow Port, Substantially Equivalent on 2017-11-14. Applicant: Lexion Medical, LLC.

Clearance details

Applicant: Lexion Medical, LLC
Product code: Code HIF
Advisory panel: Obstetrics/Gynecology
Date received: 2017-03-17
Decision date: 2017-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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.