Allergan, Inc.
FDA 510(k) & PMA Approved Devices — 32 products
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Total Devices32
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K190674 | REFRESH RELIEVA For CONTACTS | LPN | 2019-08-08 | View |
| 510(k) | K161457 | XEN Glaucoma Treatment System | KYF | 2016-11-21 | View |
| 510(k) | K083812 | REFRESH OPTIVE LENS COMFORT REWETTING DROPS | LPN | 2009-07-09 | View |
| 510(k) | K051852 | SINGLE AMPLIFIER FOR BOTOX | GWL | 2005-09-14 | View |
| 510(k) | K014202 | COMPLETE BRAND MULTI-PURPOSE SOLUTION | LPN | 2002-02-20 | View |
| 510(k) | K013479 | COMPLETE BRAND MULTI-PURPOSE SOLUTION | LPN | 2002-02-11 | View |
| 510(k) | K003252 | COMPLETE BRAND MULTI-PURPOSE SOLUTION | LPN | 2001-02-21 | View |
| 510(k) | K003638 | MOJAVE CATARACT EXTRACTION SYSTEM | HQC | 2001-02-13 | View |
| 510(k) | K003109 | COMPLETE BRAND LUBRICATING AND REWETTING DROPS | LPN | 2000-11-21 | View |
| 510(k) | K000164 | COMPLETE BRAND COMFORTPLUS MULTI-PURPOSE SOLUTION | LPN | 2000-06-02 | View |
| 510(k) | K992028 | REFRESH CONTACTS LUBRICATING AND REWETTING DROPS | LPN | 1999-10-07 | View |
| 510(k) | K984383 | ULTRACARE NEUTRALIZING TABLETS | LPN | 1998-12-18 | View |
| 510(k) | K983150 | COMPLETE BRAND LUBRICATING AND REWETTING DROPS | LPN | 1998-11-25 | View |
| 510(k) | K981168 | COMPLETE BRAND MULTI-PURPOSE SOLUTION, COMPLETE BRAND LUBRICATING AND REWETTING DROPS | LPN | 1998-09-01 | View |
| 510(k) | K980775 | COMPLETE BRAND MULTI-PURPOSE SOLUTION | LPN | 1998-07-06 | View |
| 510(k) | K981116 | SOVEREIGN CATARACT EXTRACTION SYSTEM | KYG | 1998-05-19 | View |
| 510(k) | K971186 | AMO DIPLOMAX/OPSYS CONSOLE | HQC | 1997-06-13 | View |
| 510(k) | K962402 | AMO PRESTIGE DAY PACK (ALLERGAN, INC.) | HQC | 1996-09-19 | View |
| 510(k) | K961242 | AMO PHACOFLEX II INTERSECTION SYSTEM | KYB | 1996-06-17 | View |
| 510(k) | K874543 | MODEL OPO-32 IRRIGATION SLEEVE | EIB | 1988-01-14 | View |
No matching devices.
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