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FDA 510(k)

Regular and Special Umbilical Cord Clamp and Cutter

K-Number: K152350 · 2016-06-28

ApplicantNingbo Feite Medical Device Co., Ltd.
Decision Date2016-06-28
Product CodeNBZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Regular and Special Umbilical Cord Clamp and Cutter is a medical device manufactured by Ningbo Feite Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2016-06-28 under approval number K152350. The device is classified under product code NBZ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Regular and Special Umbilical Cord Clamp and Cutter?

Regular and Special Umbilical Cord Clamp and Cutter is a medical device that received FDA 510(k) clearance on 2016-06-28. It is manufactured by Ningbo Feite Medical Device Co., Ltd.. The 510(k) number is K152350.

When was Regular and Special Umbilical Cord Clamp and Cutter approved by the FDA?

Regular and Special Umbilical Cord Clamp and Cutter received FDA 510(k) clearance on 2016-06-28, under approval number K152350.

What company makes Regular and Special Umbilical Cord Clamp and Cutter?

Regular and Special Umbilical Cord Clamp and Cutter is manufactured by Ningbo Feite Medical Device Co., Ltd..

What is the FDA product code for Regular and Special Umbilical Cord Clamp and Cutter?

The FDA product code for Regular and Special Umbilical Cord Clamp and Cutter is NBZ.

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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.

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