Johnson & Johnson Vision Care, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories1
Latest FDA decision2021-11-29
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K210930 | ACUVUE® OASYS MAX 1-DAY Contact Lenses (senofilcon A) | LPL | 2021-11-29 | View |
| 510(k) | K200243 | ACUVUE (senofilcon A) Soft Contact Lens Multifocal | LPL | 2020-03-17 | View |
| 510(k) | K180299 | ACUVUE OASYS (senofilcon A) with Photochromic Additive | LPL | 2018-04-10 | View |
| 510(k) | K160212 | ACUVUE (senofilcon C) Soft Contact Lens | LPL | 2016-03-28 | View |
No matching devices.
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