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FDA 510(k)

Regular and Special Umbilical Cord Clamp and Cutter

Numéro K : K152350 · 2016-06-28

DemandeurNingbo Feite Medical Device Co., Ltd.
Date de décision2016-06-28
Code produitNBZ
Comité consultatifOB
DécisionSubstantially Equivalent

Résumé du dispositif

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

Questions fréquentes

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. The listed applicant is Ningbo Feite Medical Device Co., Ltd.. The 510(k) number is K152350.

When did Regular and Special Umbilical Cord Clamp and Cutter receive FDA 510(k) clearance?

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

Who is the listed applicant for Regular and Special Umbilical Cord Clamp and Cutter?

The FDA 510(k) record lists Ningbo Feite Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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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Source officielle

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