Eko Scann AB

FDA Regulatory Profile

Eko Scann AB 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 March 24, 1983.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K822873DEVETHERMMarch 24, 1983
K822823HEMATOLOGY COMPUTER-INTERFACE, VISCOUNTOctober 18, 1982