EpiFaith Syringe (Luer Slip) , EpiFaith Syringe (NRFit)

FDA 510(k) K182268 · Flat Medical Co., Ltd.

Substantially Equivalent

510(k) numberK182268

Submission

Device name
EpiFaith Syringe (Luer Slip) , EpiFaith Syringe (NRFit)
Applicant
Flat Medical Co., Ltd.
Taipei, TW
Received
August 21, 2018
Decision date
April 5, 2019
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Instylla, Inc.

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K212615EpiFaith CVDQX · Traditional 09/21/2022SE
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Questions and answers

When was EpiFaith Syringe (Luer Slip) , EpiFaith Syringe (NRFit) cleared by the FDA?

EpiFaith Syringe (Luer Slip) , EpiFaith Syringe (NRFit) (K182268) received a 510(k) decision of Substantially Equivalent on April 5, 2019, 227 days after the submission was received.

What is the product code of K182268?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.