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FDA 510(k)

Sure-Fine Insulin Syringes

K-Number: K152879 · 2016-09-09

Decision Date2016-09-09
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Sure-Fine Insulin Syringes is a medical device manufactured by Shina Med Corporation. It received FDA 510(k) clearance on 2016-09-09 under approval number K152879. 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 Sure-Fine Insulin Syringes?

Sure-Fine Insulin Syringes is a medical device that received FDA 510(k) clearance on 2016-09-09. It is manufactured by Shina Med Corporation. The 510(k) number is K152879.

When was Sure-Fine Insulin Syringes approved by the FDA?

Sure-Fine Insulin Syringes received FDA 510(k) clearance on 2016-09-09, under approval number K152879.

What company makes Sure-Fine Insulin Syringes?

Sure-Fine Insulin Syringes is manufactured by Shina Med Corporation.

What is the FDA product code for Sure-Fine Insulin Syringes?

The FDA product code for Sure-Fine Insulin Syringes is FMF.

Other Devices by Shina Med Corporation

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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.