The following data is part of a premarket notification filed by Cantor & Silver Ltd. with the FDA for Cantor & Silver 5x Prosthetic Tinted (hioxifilcon A) Soft Daily Wear Contact Lens.
| Device ID | K992500 |
| 510k Number | K992500 |
| Device Name: | CANTOR & SILVER 5X PROSTHETIC TINTED (HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS |
| Classification | Lenses, Soft Contact, Daily Wear |
| Applicant | CANTOR & SILVER LTD. 623 GLACIER DR. Grand Junction, CO 81503 |
| Contact | Martin Dalsing |
| Correspondent | Martin Dalsing CANTOR & SILVER 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 | 1999-07-26 |
| Decision Date | 1999-08-18 |
| Summary: | summary |