Fehling Instruments GmbH & Co. KG

FDA Regulatory Profile

Fehling Instruments GmbH & Co. KG appears in FDA public data with 0 recalls, 2 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 2, 2017.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K170726Biopsy ForcepsJune 2, 2017
K153243Fehling-PunchesAugust 4, 2016