Oves Cervical Cap
FDA 510(k) K993953 · Veos , Ltd.
510(k) numberK993953
Submission
- Device name
- Oves Cervical Cap
- Applicant
- Veos , Ltd.
Lake Forest, IL, US - Received
- November 22, 1999
- Decision date
- March 21, 2000
- Decision
- Unknown (SESU)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- HDR – Cap, Cervical
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.5250
- Specialty
- Obstetrics/Gynecology
Other 510(k)s with product code HDR
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K242031 | Béa Applicator (BAP-GB-01)HDR · Traditional | Stepone Fertility Ltd (T/A Béa Fertility) | 04/02/2025SE |
| K222969 | FERTI-LILY Conception CupHDR · Traditional | Rosesta Medical BV | 06/23/2023SE |
| K945131 | Imagyn Intrauterine Insemination DeviceHDR · Traditional | Imagyn Medical, Inc. | 05/15/1995SE |
| K950714 | Cook Insemination CupHDR · Traditional | Cook Urological, Inc. | 05/11/1995SE |
| K902171 | Minispace(Tm) Iui CatheterHDR · Traditional | Pharmacia, Inc. | 10/05/1990SE |
| K902694 | Coaxial Catheter SetHDR · Traditional | Cook Ob/Gyn | 08/28/1990SE |
| K896960 | Intrauterine Insemination CathetersHDR · Traditional | C.R. Bard, Inc. | 06/26/1990SE |
| K900316 | Modified Ham's F-10 Medium and Medium-HepesHDR · Traditional | Irvine Scientific | 04/16/1990SE |
| K900308 | Sperm Select SystemHDR · Traditional | Pharmacia, Inc. | 04/13/1990SE |
| K900162 | DGH A-San Probe HolderHDR · Traditional | Jedmed Instrument Co. | 02/16/1990SE |
Questions and answers
When was Oves Cervical Cap cleared by the FDA?
Oves Cervical Cap (K993953) received a 510(k) decision of Unknown on March 21, 2000, 120 days after the submission was received.
What is the product code of K993953?
The FDA product code is HDR – Cap, Cervical, a Class II (moderate risk) device regulated under 21 CFR 884.5250.