510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K152350Substantially Equivalent

Regular and Special Umbilical Cord Clamp and Cutter

Ningbo Feite Medical Device Co., Ltd., Ningbo, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K152350 is the FDA 510(k) clearance record for Regular and Special Umbilical Cord Clamp and Cutter, a class II device, cleared for Ningbo Feite Medical Device Co., Ltd. on under FDA product code NBZ (Clamp And Cutter, Umbilical). FDA records list one 510(k) clearance for Ningbo Feite Medical Device Co., Ltd. As of , FDA records show no recalls naming K152350.

Clearance record

Decision date
Received
(313 days to decision)
Product code
NBZ Clamp And Cutter, Umbilical
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Ningbo Feite Medical Device Co., Ltd. Tongpenzha, Zhonggongmiao St., Yinzhou District, Ningbo, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NBZ

Trailing 12 months

FDA records hold no clearances under product code NBZ in the trailing twelve months.

FDA records show no clearances under product code NBZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NBZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260