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FDA 510(k)

Vesco Medical NRFit Tip Syringes

K-Number: K170218 · 2017-02-24

Decision Date2017-02-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Vesco Medical NRFit Tip Syringes is the device name listed in this FDA 510(k) record. The listed applicant is Vesco Medical, LLC. It received FDA 510(k) clearance on 2017-02-24 under 510(k) number K170218. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vesco Medical NRFit Tip Syringes?

Vesco Medical NRFit Tip Syringes is a medical device that received FDA 510(k) clearance on 2017-02-24. The listed applicant is Vesco Medical, LLC. The 510(k) number is K170218.

When did Vesco Medical NRFit Tip Syringes receive FDA 510(k) clearance?

Vesco Medical NRFit Tip Syringes received FDA 510(k) clearance on 2017-02-24, under 510(k) number K170218.

Who is the listed applicant for Vesco Medical NRFit Tip Syringes?

The FDA 510(k) record lists Vesco Medical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vesco Medical NRFit Tip Syringes?

The FDA product code for Vesco Medical NRFit Tip Syringes is FMF.

Other records listing Vesco Medical, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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