KRF — Charger, Pacemaker Class I
FDA product code KRF covers "Charger, Pacemaker", a Class I medical device regulated under 21 CFR 870.3670. Submissions are reviewed by the Cardiovascular panel.
Classification Details
- Product Code
- KRF
- Device Class
- Class I
- Regulation Number
- 870.3670
- Submission Type
- Review Panel
- CV
- Medical Specialty
- Cardiovascular
- Implant
- No