DEVICE, FEMALE INCONTINENCE— 510(k) K781863

Unknown

Eschmann Bros. & Walsh , Ltd.

FDA 510(k) clearance K781863 for DEVICE, FEMALE INCONTINENCE, Unknown on 1978-11-06. Applicant: Eschmann Bros. & Walsh , Ltd..

Clearance details

Applicant: Eschmann Bros. & Walsh , Ltd.
Product code: Code HHW
Advisory panel: Obstetrics/Gynecology
Date received: 1978-11-06
Decision date: 1978-11-06
Decision: Unknown
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HHW

product code HHW

Malfunction: 485
Total: 485

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.