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Medlog GmbH Marketing Services

FDA Regulatory Profile

Medlog GmbH Marketing Services appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 19, 1983.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K832086USE 77 ULTRASONIC NEBULIZERJuly 19, 1983
K831325NUTROMATJune 2, 1983
K830913MINITROP AEROSAL, PRODOMO AEROSAL ANDMay 25, 1983
K813455PUMP & DETECTORJanuary 5, 1982
K810155DOP 84May 1, 1981

FDA data resources