The following data is part of a premarket notification filed by Seinoh Optical Co. Ltd. with the FDA for Ilens (ocufilcon D) Daily Soft Contact Lens.
Device ID | K141280 |
510k Number | K141280 |
Device Name: | ILENS (OCUFILCON D) DAILY SOFT CONTACT LENS |
Classification | Lenses, Soft Contact, Daily Wear |
Applicant | SEINOH OPTICAL CO. LTD. 6F, NO. 39, LN 224, JIXIAN RD, LUZHOU DIST. New Taipei City, TW 247 |
Contact | Jennifer Ting |
Correspondent | Jennifer Ting SEINOH OPTICAL CO. LTD. 6F, NO. 39, LN 224, JIXIAN RD, LUZHOU DIST. New Taipei City, TW 247 |
Product Code | LPL |
CFR Regulation Number | 886.5925 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-05-16 |
Decision Date | 2014-07-18 |
Summary: | summary |