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Marvic Interpharma, Inc.

FDA Regulatory Profile

Marvic Interpharma, Inc. 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 April 4, 1986.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K854223VES-TEC/VES-MATICApril 4, 1986
K854222DIESSE RF TEST KITFebruary 6, 1986
K854221DIESSE CRP TEST KITNovember 25, 1985

FDA data resources