The following data is part of a premarket notification filed by Visioneering Technologies, Inc. with the FDA for Naturalvue (etafilcon A) Daily Disposable Soft (hydrophilic) Contact Lenses.
Device ID | K150385 |
510k Number | K150385 |
Device Name: | NaturalVue (etafilcon A) Daily Disposable Soft (Hydrophilic) Contact Lenses |
Classification | Lenses, Soft Contact, Daily Wear |
Applicant | Visioneering Technologies, Inc. 4555 Mansell Road Suite 300 Alpharetta, GA 30022 |
Contact | Stephen Snowdy |
Correspondent | Penny Northcutt REGSolutions, LLC 174 Watercolor Way Suite 103-403 Santa Rosa Beach, FL 32459 |
Product Code | LPL |
CFR Regulation Number | 886.5925 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-02-18 |
Decision Date | 2015-04-30 |
Summary: | summary |