Product code MRP— Anesthesiology
VIANOX DELIVERY SYSTEM, MODEL I
- Classification name
- Analyzer, Nitric Oxide
- Device class
- Class 2
- Regulation
- 21 CFR 868.2380
- Advisory panel
- Anesthesiology
- Total cleared
- 1
- First cleared
- Most recent
Market context for product code MRP
FDA has cleared device under product code MRP, all in 2003, filed by 1 applicant company. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Top applicants under product code MRP
Recent clearances under product code MRP
Data sourced from openFDA. This site is unofficial and independent of the FDA.