Eschmann Bros. & Walsh , Ltd.

Eschmann Bros. & Walsh , Ltd. holds 3 FDA 510(k) medical device clearances, first cleared 1978, most recent 1987.

Top product codes for Eschmann Bros. & Walsh , Ltd.

GEI — General, Plastic Surgery1 device
HHW — Obstetrics/Gynecology1 device

Recent clearances by Eschmann Bros. & Walsh , Ltd.

K864637 — MODIFIED ESCHMANN DILATATION CATHETER·1987-01-06
K852935 — ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411Code GEI·1985-10-10
K781863 — DEVICE, FEMALE INCONTINENCECode HHW·1978-11-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.