inforMED
DWJClass II

System, Thermal Regulating

Cardiovascular · 21 CFR 870.5900

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

MDR events26,611All time
Recalls70All time
Registered firms175Currently listed
510(k) clearances160All time

Recalls

70 recall events for this product code

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