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

Instrument, Destructive, Fetal, Obstetric

21 CFR 884.4500 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

KNB is the FDA product code for Instrument, Destructive, Fetal, Obstetric, a class II device type, regulated under 21 CFR 884.4500. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KNB
Device name
Instrument, Destructive, Fetal, Obstetric
Regulation
21 CFR 884.4500
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
1
Ingested recalls
0

Clearances, product code KNB

By decision year
1 clearance under product code KNB with a decision year between 1989 and 1989, 1989 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KNB by decision year
YearClearances
19891

Applicants with the most clearances

Product code KNB
Applicants holding the most 510(k) clearances under product code KNB
ApplicantClearances
Kinetic Medical Products1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code KNB.