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KIO — Slide Stainer, Immersion Type Class I

FDA Device Classification

Classification Details

Product Code: KIO
Device Class: Class I
Regulation Number: 864.3800
Submission Type
Review Panel: PA
Medical Specialty: Pathology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K890984	shandon	LINISTAIN SLS	April 4, 1989