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FDA 510(k)

MHC Standard and NRFit Tip Syringes

K-Number: K171131 · 2017-11-08

Decision Date2017-11-08
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MHC Standard and NRFit Tip Syringes is a medical device manufactured by Mazza Healthcare, LLC. It received FDA 510(k) clearance on 2017-11-08 under approval number K171131. 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 MHC Standard and NRFit Tip Syringes?

MHC Standard and NRFit Tip Syringes is a medical device that received FDA 510(k) clearance on 2017-11-08. It is manufactured by Mazza Healthcare, LLC. The 510(k) number is K171131.

When was MHC Standard and NRFit Tip Syringes approved by the FDA?

MHC Standard and NRFit Tip Syringes received FDA 510(k) clearance on 2017-11-08, under approval number K171131.

What company makes MHC Standard and NRFit Tip Syringes?

MHC Standard and NRFit Tip Syringes is manufactured by Mazza Healthcare, LLC.

What is the FDA product code for MHC Standard and NRFit Tip Syringes?

The FDA product code for MHC Standard and NRFit Tip Syringes is FMF.

Related Clinical Trials

Related Devices (Code: FMF)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.