The following data is part of a premarket notification filed by Coopervision, Inc. with the FDA for Frequency 38 And Silver 07 (polymacon) Soft (hydrophilic) Contact Lens.
Device ID | K042824 |
510k Number | K042824 |
Device Name: | FREQUENCY 38 AND SILVER 07 (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS |
Classification | Lenses, Soft Contact, Daily Wear |
Applicant | COOPERVISION, INC. 711 NORTH RD. Scottsville, NY 14546 |
Contact | Bonnie J Tsymbal |
Correspondent | Bonnie J Tsymbal COOPERVISION, INC. 711 NORTH RD. Scottsville, NY 14546 |
Product Code | LPL |
CFR Regulation Number | 886.5925 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-10-12 |
Decision Date | 2004-11-16 |
Summary: | summary |