KNH — Laparoscopic Contraceptive Tubal Occlusion Device Class III

FDA Device Classification

Classification Details

Product Code
KNH
Device Class
Class III
Regulation Number
884.5380
Submission Type
Review Panel
OB
Medical Specialty
Obstetrics/Gynecology
Implant
Yes

Definition

Call for PMAs to be filed by 12/30/87 (52 FR 36883 (10/1/87))