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LOO — Reagent, Leishmanii Serological Class I

FDA Device Classification

Classification Details

Product Code
LOO
Device Class
Class I
Regulation Number
866.3870
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K023483inbios intlKALAZAR DETECTMay 6, 2003
K842526amico labAMIZYME-LEISHMANIA SPP. TEST KITAugust 28, 1984