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GRD — Antiserum, Hai, Mumps Virus Class I

FDA Device Classification

Classification Details

Product Code
GRD
Device Class
Class I
Regulation Number
866.3380
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K833077wellcome diagnosticsWELLCOGEN H. INFLUENZAL ZL21January 10, 1984