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MJK — Dna Probe, Trichomonas Vaginalis Class I

FDA Device Classification

Classification Details

Product Code: MJK
Device Class: Class I
Regulation Number: 866.2660
Submission Type
Review Panel: MI
Medical Specialty: Microbiology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K922457	microprobe	AFFIRM VP MICROBIAL ID TEST FOR TRICHOMONAS VAGINA	September 25, 1992