MOQ — Battery, Replacement, Rechargeable Class I
FDA Device Classification
Classification Details
- Product Code
- MOQ
- Device Class
- Class I
- Regulation Number
- 878.4820
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K081713 | vidacare corporation | VERTEBRAL ACCESS SYSTEM BY VIDACARE | November 21, 2008 |
| K013133 | nordix | NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 | November 13, 2001 |
| K980224 | alexander mfg | ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822 | April 2, 1998 |