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1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Antigen, Cf, Q Fever
Device class
Class I (low risk)
Regulation
21 CFR 866.3500
Medical specialty
Microbiology
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RecordFirmDate
Q-FEVER (K843672)Institute Virion , Ltd.1985-08-08

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Every clearance here is in the API, with alerts when new ones post.