CFA — Electrode, Ion Specific, Magnesium Class I
FDA Device Classification
Classification Details
- Product Code
- CFA
- Device Class
- Class I
- Regulation Number
- 862.1495
- Submission Type
- Review Panel
- CH
- Medical Specialty
- Clinical Chemistry
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K863267 | data medical associates | MAGNESIUM PROCEDURE | September 11, 1986 |
| K851514 | bio-analytics laboratories | ULTRA-VIOLET GLUCOSE REAGENT | May 20, 1985 |