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Ganshorn Medizin Electronic GmbH

FDA Regulatory Profile

Ganshorn Medizin Electronic GmbH 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 December 9, 2024.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K240706PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PoDecember 9, 2024
K160116SpiroScoutOctober 7, 2016

FDA data resources