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FDA 510(k) Applications for Medical Device Product Code "QBF"
FDA 510(k) Number
Applicant
Device Name
Decision Date
K210327
W.H.P.M., Inc.
First Sign Multi-Drug Test Dip Card, First Sign Multi-Drug Test Cup, First Sign Multi-Drug Screen Test Dip Card, First Sign Multi-Drug Screen Test Cup
08/12/2021
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