FDA Product Code
FDA Product Code MOQ — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- General, Plastic Surgery
- 21 CFR Citation
- 878.4820
510(k) Clearances — 3 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K081713 | VERTEBRAL ACCESS SYSTEM BY VIDACARE | Vidacare Corporation | 2008-11-21 | Traditional | PDF ↗ |
| K013133 | NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 | Nordix, Inc. | 2001-11-13 | Traditional | PDF ↗ |
| K980224 | ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822 | Alexander Mfg. Co. | 1998-04-02 | Traditional | PDF ↗ |
Product code MOQ · Class I · General, Plastic Surgery. Data: openFDA.