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

Set, Anesthesia, Obstetric

21 CFR 884.5100 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

KNE is the FDA product code for Set, Anesthesia, Obstetric, a class II device type, regulated under 21 CFR 884.5100. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KNE
Device name
Set, Anesthesia, Obstetric
Regulation
21 CFR 884.5100
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code KNE

By decision year
2 clearances under product code KNE with a decision year between 1986 and 1988, 1986 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KNE by decision year
YearClearances
19861
19881

Applicants with the most clearances

Product code KNE
Applicants holding the most 510(k) clearances under product code KNE
ApplicantClearances
BD Becton Dickinson Vacutainer Systems Preanalytic1
Hdc Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code