Johnson & Johnson Consumer Companies, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K062602 | BAND-AID(R) BRAND LIQUID BANDAGE | KMF | 2006-12-11 | View |
| 510(k) | K001023 | FREEDOM, MODEL 4660 | SEJ | 2000-09-22 | View |
No matching devices.
Advertisement