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GRD

1 FDA 510(k) clearances · Product code

FDA profile

Official device name
Antiserum, Hai, Mumps Virus
Device class
Class I (low risk)
Regulation
21 CFR 866.3380
Medical specialty
Microbiology
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RecordFirmDate
WELLCOGEN H. INFLUENZAL ZL21 (K833077)Wellcome Diagnostics1984-01-10

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