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LQA — Media, Reusable Image Class I

FDA Device Classification

Classification Details

Product Code: LQA
Device Class: Class I
Regulation Number: 892.1840
Submission Type
Review Panel: RA
Medical Specialty: Radiology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K854407	digirad	DIGIRAD REUSABLE IMAGE MEDIA	March 10, 1986