Surflo Winged Infusion Set

FDA 510(k) K221411 · Terumo Medical Products (Hangzhou) Co., Ltd.

Substantially Equivalent

510(k) numberK221411

Submission

Device name
Surflo Winged Infusion Set
Applicant
Terumo Medical Products (Hangzhou) Co., Ltd.
Hangzhou, CN
Received
May 16, 2022
Decision date
June 23, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FPA – Set, Administration, Intravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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Questions and answers

When was Surflo Winged Infusion Set cleared by the FDA?

Surflo Winged Infusion Set (K221411) received a 510(k) decision of Substantially Equivalent on June 23, 2023, 403 days after the submission was received.

What is the product code of K221411?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.