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Device, Female Incontinence

by Eschmann Bros. & Walsh, Ltd. 510(k)

Active United States

510(k) K781863

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESP Substantially Equivalent — Postmarket Surveillance · Traditional NumberK781863 Date6 Nov 1978ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 10 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
HHW
FDA applicant
Eschmann Bros. & Walsh , Ltd.
Device Class
Class II
Regulation
21 CFR Part 884.3575
Advisory Committee
Obstetrics/Gynecology
FDA Decision
SESP Substantially Equivalent — Postmarket Surveillance

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