LHP — System, Telethermographic (Sole Diagnostic Screen) Class III
FDA product code LHP covers "System, Telethermographic (Sole Diagnostic Screen)", a Class III medical device regulated under 21 CFR 884.2980. Submissions are reviewed by the Obstetrics/Gynecology panel.
Classification Details
- Product Code
- LHP
- Device Class
- Class III
- Regulation Number
- 884.2980
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No