KNH — Laparoscopic Contraceptive Tubal Occlusion Device Class III
FDA product code KNH covers "Laparoscopic Contraceptive Tubal Occlusion Device", a Class III medical device regulated under 21 CFR 884.5380. Submissions are reviewed by the Obstetrics/Gynecology panel. Devices under this code are implants.
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))