KDW

4 FDA 510(k) clearances · Product code

FDA profile

Official device name

Container, Specimen Mailer And Storage, Temperature Controlled, Sterile

Device class

Class I (low risk)

Regulation

21 CFR 864.3250

Medical specialty

Pathology

Adverse events (MAUDE)

1995: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.

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