Interlab S.R.L.

FDA Regulatory Profile

Interlab S.R.L. appears in FDA public data with 0 recalls, 4 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on June 30, 2006.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K053571MICROGEL ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM, MICROGEL ACID HEMOGLOBIN ELECTROPHORESIS TJune 30, 2006
K040146INTERLAB ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEMMay 4, 2004
K032862INTERLAB ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEMFebruary 3, 2004
K033187INTERLAB IMMUNOFIXATION TEST(S)November 19, 2003