Moxxly Flow Collection System— 510(k) K170722

Substantially Equivalent

Moxxly, Inc.

FDA 510(k) clearance K170722 for Moxxly Flow Collection System, Substantially Equivalent on 2017-08-28. Applicant: Moxxly, Inc..

Clearance details

Applicant: Moxxly, Inc.
Product code: Code HGX
Advisory panel: Obstetrics/Gynecology
Date received: 2017-03-09
Decision date: 2017-08-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HGX

product code HGX

Injury: 758
Other: 2
Total: 760

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.