Gelflex Laboratories · Class II · Cleared Apr 1, 2003
| K-number | K030027 |
| Device name | GELFLEX SYNERGY SOFT LENS HIOXFILCON 49% WATER CONTENT CLEAR OR BLUE VISITINT; GELFLEX HIOXIFILCON SOFT CONTACT LENS 49% |
| Applicant | Gelflex Laboratories |
| Product code | LPL |
| Device class | Class II |
| Decision date | Apr 1, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 886.5925 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov