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Hennig Enterprises Europe Srl

FDA Regulatory Profile

Hennig Enterprises Europe Srl appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 29, 2003.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K020424V SETAugust 29, 2003
K020421GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICESApril 29, 2003

FDA data resources