The following data is part of a premarket notification filed by Cantor & Nissel Ltd. with the FDA for Cantor & Nissel Hand Painted Prosthetic Soft Contact Lens For Daily Wear.
Device ID | K041700 |
510k Number | K041700 |
Device Name: | CANTOR & NISSEL HAND PAINTED PROSTHETIC SOFT CONTACT LENS FOR DAILY WEAR |
Classification | Lenses, Soft Contact, Daily Wear |
Applicant | CANTOR & NISSEL LTD. 623 GLACIER DR. Grand Juction, CO 81503 |
Contact | Martin Dalsing |
Correspondent | Martin Dalsing CANTOR & NISSEL LTD. 623 GLACIER DR. Grand Juction, 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 | 2004-06-22 |
Decision Date | 2004-07-30 |
Summary: | summary |