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FDA 510(k) Applications for Medical Device Product Code "GRZ"
(Antisera, Fluorescent, All, Mycoplasma Spp.)
FDA 510(k) Number
Applicant
Device Name
Decision Date
K946373
ZEUS SCIENTIFIC, INC.
MYCOPLASMA SLURRY AND MYCOPLASMA CROWNTITRE IFA TEST SYSTEM
02/07/1996
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