Blood Vessel Connector
FDA 510(k) K871408 · Quali-Med, Inc.
510(k) numberK871408
Submission
- Device name
- Blood Vessel Connector
- Applicant
- Quali-Med, Inc.
Stafford, TX, US - Received
- April 8, 1987
- Decision date
- April 27, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Quali-Med, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K862972 | Disposable Mirror · Traditional | 09/23/1986SE |
| K862472 | Quartz Rods Titanium RodsGEX · Traditional | 09/12/1986SE |
| K862241 | Standard Basin Kit Custom Basin KitFRG · Traditional | 08/01/1986SE |
| K862242 | Pap Smear KitHHT · Traditional | 06/26/1986SE |
| K862172 | Quali-Med's Operating Room DrapesKKX · Traditional | 06/19/1986SE |
| K861198 | Custom Procedure Kit (Various Sub-Titles) · Traditional | 05/16/1986SESD |
Questions and answers
When was Blood Vessel Connector cleared by the FDA?
Blood Vessel Connector (K871408) received a 510(k) decision of Substantially Equivalent on April 27, 1987, 19 days after the submission was received.