The following data is part of a premarket notification filed by Veos Ltd. with the FDA for Oves Cervical Cap.
| Device ID | K993953 |
| 510k Number | K993953 |
| Device Name: | OVES CERVICAL CAP |
| Classification | Cap, Cervical |
| Applicant | VEOS LTD. 273 MARKET SQUARE CT., #12 Lake Forest, IL 60045 |
| Contact | Peggy S Dannenbaum |
| Correspondent | Peggy S Dannenbaum VEOS LTD. 273 MARKET SQUARE CT., #12 Lake Forest, IL 60045 |
| Product Code | HDR |
| CFR Regulation Number | 884.5250 [🔎] |
| Decision | Se - With Limitations (SESU) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-11-22 |
| Decision Date | 2000-03-21 |