Product code OFH
- Device name
- Digital Angiography Tray
- Medical specialty
- Cardiovascular
- Device class
- 2
- Regulation number
- 870.1650
- Review panel
- CV
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Definition
- This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.
- Source
- FDA openFDA device classification dataset
Related GUDID Devices
| Primary DI | Brand | Company | Published |
|---|
| 50197106807925 | CARDINAL HEALTH | Cardinal Health 200, LLC | 2024-12-11 |
| 50197106636310 | CARDINAL HEALTH | Cardinal Health 200, LLC | 2024-07-10 |
| 50197106220090 | CARDINAL HEALTH | Cardinal Health 200, LLC | 2023-05-11 |
| 50195594385628 | CARDINAL HEALTH | Cardinal Health 200, LLC | 2021-10-15 |