Ocutec Corporation, Inc. · Class II · Cleared Aug 5, 1994
| K-number | K942533 |
| Device name | NOVALENS/NOVAWET PERCEPTION AND VANGUARD |
| Applicant | Ocutec Corporation, Inc. |
| Product code | HQD |
| Device class | Class II |
| Decision date | Aug 5, 1994 |
| Decision | Substantially Equivalent |
| Regulation | 886.5916 |
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