OVES CERVICAL CAP— 510(k) K993953
UnknownVeos , Ltd.
FDA 510(k) clearance K993953 for OVES CERVICAL CAP, Unknown on 2000-03-21. Applicant: Veos , Ltd.. Device class: 2.
Clearance details
- Applicant
- Veos , Ltd.
- Product code
- Code HDR
- Device class
- Class 2
- Regulation
- 21 CFR 884.5250
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Lake Forest, IL, US
Recent devices under product code HDR
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