JED — Analyzer, Oxyhemoglobin Concentration, Blood-Phase, Indwelling Class III
FDA product code JED covers "Analyzer, Oxyhemoglobin Concentration, Blood-Phase, Indwelling", a Class III medical device regulated under 21 CFR 868.1120. Submissions are reviewed by the Anesthesiology panel.
Classification Details
- Product Code
- JED
- Device Class
- Class III
- Regulation Number
- 868.1120
- Submission Type
- Review Panel
- AN
- Medical Specialty
- Anesthesiology
- Implant
- No
Definition
A PMA or notice of completion of a PDP is required to be filed with the Food and Drug Administration on or before September 21, 2004, for any indwelling blood oxyhemoglobin concentration analyzer that was in commercial distribution before May 28, 1976, or that has, on or before September 21, 2004, been found to be substantially equivalent to an indwelling blood oxyhemoglobin concentration analyzer that was in commercial distribution before May 28, 1976. Any other indwelling blood oxyhemoglobin concentration analyzer shall have an approved PMA or declared completed PDP in effect before being placed in commercial distribution.