510(k) K200389
K200389 is an FDA 510(k) premarket notification submitted by Mallinckrodt Manufacturing, LLC for the device "INOmax DSIR Plus". The FDA issued a decision of Substantially Equivalent on June 17, 2020. The device falls under product code MRN (Apparatus, Nitric Oxide Delivery), a Class II device regulated under 21 CFR 868.5165. Mallinckrodt Manufacturing, LLC has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 17, 2020
- Date Received
- February 18, 2020
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Apparatus, Nitric Oxide Delivery
- Device Class
- Class II
- Regulation Number
- 868.5165
- Review Panel
- AN
- Submission Type