The following data is part of a premarket notification filed by Contamac Ltd. with the FDA for Contaflex Gm3 58% (acofilcon A) Spherical Soft Contact Lens For Daily Wear (clear And Tinted, Lathe-cut).
Device ID | K023349 |
510k Number | K023349 |
Device Name: | CONTAFLEX GM3 58% (ACOFILCON A) SPHERICAL SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, LATHE-CUT) |
Classification | Lenses, Soft Contact, Daily Wear |
Applicant | CONTAMAC LTD. 623 GLACIER DR. Grand Junction, CO 81503 |
Contact | Martin Dalsing |
Correspondent | Martin Dalsing CONTAMAC LTD. 623 GLACIER DR. Grand Junction, CO 81503 |
Product Code | LPL |
CFR Regulation Number | 886.5925 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-10-07 |
Decision Date | 2002-12-24 |
Summary: | summary |