JXF — Plethysmograph, Ocular Class III
FDA product code JXF covers "Plethysmograph, Ocular", a Class III medical device regulated under 21 CFR 882.1790. Submissions are reviewed by the Neurology panel.
Classification Details
- Product Code
- JXF
- Device Class
- Class III
- Regulation Number
- 882.1790
- Submission Type
- Review Panel
- NE
- Medical Specialty
- Neurology
- Implant
- No
Definition
PMAs to be filed by 9/21/04 (69 FR 34920 (6/23/04))