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CBG — Spreader, Cuff Class I

FDA Device Classification

Classification Details

Product Code: CBG
Device Class: Class I
Regulation Number: 868.5760
Submission Type
Review Panel: AN
Medical Specialty: Anesthesiology
Implant: No

Recent 510(k) Clearances

K-Number	Applicant	Device Name	Date
K870600	kalajian ent	SOFT EAR STETHOSCOPE	March 19, 1987