Pfm Produkte Fur Die Medizin AG

FDA Regulatory Profile

Pfm Produkte Fur Die Medizin AG appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 24, 2002.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K011783MULTI-SNARE SETJanuary 24, 2002
K002471JETCAN HUBER NEEEDLE SETOctober 19, 2000
K001716REDON SETJuly 19, 2000