FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AeroNOx 2.0 Nitric Oxide Titration & Monitoring System
K Number: K193481
·
Decision Mar 10, 2020
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
32
Applicant Total
8
Review Days
84
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Basic Information
- Device Name
- AeroNOx 2.0 Nitric Oxide Titration & Monitoring System
- K Number
- K193481
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 868.5165
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- International Biomedical
- Date Received
- December 17, 2019
- Decision Date
- March 10, 2020
- Product Code
- MRN
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MRN | Apparatus, Nitric Oxide Delivery | FDA class 2 | Anesthesiology |
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