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IWW — Shield, Vial Class I

FDA Device Classification

Classification Details

Product Code: IWW
Device Class: Class I
Regulation Number: 892.6500
Submission Type
Review Panel: RA
Medical Specialty: Radiology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K934548	victoreen	ALL-VUE & GAMMA-VUE VIAL SHIELDS	November 12, 1993