HIQ — Electrode, Clip, Fetal Scalp (And Applicator) Class III

FDA Device Classification

Classification Details

Product Code
HIQ
Device Class
Class III
Regulation Number
884.2685
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
No

Definition

Call for PMAs to be filed by 12/26/96 per 61 FR 50708 on 9/27/96