510(k) K221411
K221411 is an FDA 510(k) premarket notification submitted by Terumo Medical Products (Hangzhou) Co., Ltd. for the device "Surflo Winged Infusion Set". The FDA issued a decision of Substantially Equivalent on June 23, 2023. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Terumo Medical Products (Hangzhou) Co., Ltd. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 23, 2023
- Date Received
- May 16, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Set, Administration, Intravascular
- Device Class
- Class II
- Regulation Number
- 880.5440
- Review Panel
- HO
- Submission Type