510(k) K082880
K082880 is an FDA 510(k) premarket notification submitted by I-See Vision Technology, Inc. for the device "EZVUE (OCUFILCON D) 1-DAY SOFT (HYDROPHILIC)CONTACT LENS". The FDA issued a decision of Substantially Equivalent on Jun 16, 2009. The device falls under product code LPL (Lenses, Soft Contact, Daily Wear), a Class II device regulated under 21 CFR 886.5925. I-See Vision Technology, Inc. has 3 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jun 16, 2009
- Date Received
- Sep 29, 2008
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Lenses, Soft Contact, Daily Wear
- Device Class
- Class II
- Regulation Number
- 886.5925
- Review Panel
- OP
- Submission Type
- 510(k)