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

Clamp And Cutter, Umbilical

21 CFR 884.4530 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

NBZ is the FDA product code for Clamp And Cutter, Umbilical, a class II device type, regulated under 21 CFR 884.4530. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
NBZ
Device name
Clamp And Cutter, Umbilical
Regulation
21 CFR 884.4530
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code NBZ

By decision year
1 clearance under product code NBZ with a decision year between 2016 and 2016, 2016 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NBZ by decision year
YearClearances
20161

Applicants with the most clearances

Product code NBZ
Applicants holding the most 510(k) clearances under product code NBZ
ApplicantClearances
Ningbo Feite Medical Device Co., Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code