Perstorp AB C/O Robert Joel Slomoff

FDA Regulatory Profile

Perstorp AB C/O Robert Joel Slomoff 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 January 31, 1991.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K905069IODOSORB GELJanuary 31, 1991
K870559IODOSORB POWDERMarch 20, 1987