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Goosen Enterprises, Inc.

FDA Regulatory Profile

Goosen Enterprises, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 18, 1994.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K923848GOOSEN SELF-LUBRICATING CATHETERFebruary 18, 1994
K896134ACUFLO, VACUUM-POWERED BODY FLUID SUCTION APPARA.August 30, 1990
K896579GOOSEN URINARY DRAINAGE SYSTEMFebruary 15, 1990
K844889MENSINK-GOOSEN CATHETERMarch 18, 1985

FDA data resources