ClearanceBrief
Company ยท US

Alcon, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2008. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LPNAccessories, Soft Lens Products3
HQCUnit, Phacofragmentation1
LZUPlug, Punctum1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 9, 2008K063583ALCON VISION SYSTEM
Alcon
HQC
Dec 12, 2007K071236ALCON MULTI-PURPOSE SOLUTION
Alcon, Inc.
LPN
Jul 13, 2004K040231INTELIPORT OCCLUDING DEVICE
Alcon, Inc.
LZU
Jul 3, 2003K031193SOFT (HYDROPHILIC) CONTACT LENS CARE SOLUTION
Alcon, Inc.
LPN
Jul 6, 1998K981574OPTI-FREE EXPRESS MULTI-PURPOSE SOLUTION
Alcon
LPN

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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