Vesco Medical NRFit Tip Syringes

FDA 510(k) K170218 · Vesco Medical, LLC

Substantially Equivalent

510(k) numberK170218

Submission

Device name
Vesco Medical NRFit Tip Syringes
Applicant
Vesco Medical, LLC
Columbus, OH, US
Received
January 25, 2017
Decision date
February 24, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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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Questions and answers

When was Vesco Medical NRFit Tip Syringes cleared by the FDA?

Vesco Medical NRFit Tip Syringes (K170218) received a 510(k) decision of Substantially Equivalent on February 24, 2017, 30 days after the submission was received.

What is the product code of K170218?

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