HEJ — Monitor, Hemic Sound, Ultrasonic Class II
FDA product code HEJ covers "Monitor, Hemic Sound, Ultrasonic", a Class II medical device regulated under 21 CFR 884.2660. Submissions are reviewed by the Obstetrics/Gynecology panel.
Classification Details
- Product Code
- HEJ
- Device Class
- Class II
- Regulation Number
- 884.2660
- Submission Type
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No