OBI
2019-09-13
Catheter, Pressure Monitoring, Cardiac
FDA product code OBI · 1 cleared devices
Class 2
Cardiovascular
- Regulation
- 21 CFR 870.1200
- Review panel
- CV
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2019-09-13 – 2019-09-13
To measure pressure within the cardiovascular system.
No matching devices.
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