MWZ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Expander, Breast, External
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.5660
- Medical specialty
- Physical Medicine
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SALONMAY BUSTLINE INCREASER (K770082) | Gamma Enterprises, Inc. | 1977-03-16 |
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