Product code OFB
- Device name
- Catheter Guide Wire Kit
- Medical specialty
- Cardiovascular
- Device class
- 2
- Regulation number
- 870.1330
- 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 http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. 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 |
|---|
| 10886333200006 | Vascular Kit | ARGON MEDICAL DEVICES, INC. | 2016-09-21 |