HRDClass II
Sterilizer, Soft-lens, Thermal, Ac-powered
Ophthalmic · 21 CFR 886.5928
MDR events8All time
Recalls0All time
Registered firms0Currently listed
510(k) clearances1All time
Recent MDR events
8 adverse event reports on file
- ALLERGAN CUP (GORETEX)Oct 27, 2005MalfunctionAllergan, Inc.2020664-2005-00027
- ALLERGAN CUP (GORETEX)Oct 27, 2005MalfunctionAllergan, Inc.2020664-2005-00028
- ALLERGAN CUP (GORETEX)Oct 27, 2004MalfunctionAllergan, Inc.2020664-2004-00025
- ALLERGAN CUP (GORETEX)Oct 27, 2004MalfunctionAllergan, Inc.2020664-2004-00026
- ALLERGAN CUP (GORETEX)Jan 28, 2000MalfunctionAllergan2011068-1999-00017
- ALLERGAN CUP (GORETEX)Jan 28, 2000MalfunctionAllergan2011068-1999-00016
- AOSEPT LENS CUPAug 7, 1997MalfunctionCiba Vision Corp.1053053-1997-00001
- ALLERGAN CUPApr 30, 1997InjuryAllergan Optical2011068-1997-00039
Event type breakdown
Malfunction7
Injury1
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
0 firms currently registered for this product code
No registered firms found for this product code.
510(k) clearances
1 clearances for this product code