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

Adapter, A-V Shunt Or Fistula

21 CFR 876.5540 / Gastroenterology, Urology
FDA source (opens on fda.gov)

KNR is the FDA product code for Adapter, A-V Shunt Or Fistula, a class II device type, regulated under 21 CFR 876.5540. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
KNR
Device name
Adapter, A-V Shunt Or Fistula
Regulation
21 CFR 876.5540
Device class
Class II
Review panel
Gastroenterology, Urology
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code KNR

By decision year
1 clearance under product code KNR with a decision year between 1981 and 1981, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KNR by decision year
YearClearances
19811

Applicants with the most clearances

Product code KNR
Applicants holding the most 510(k) clearances under product code KNR
ApplicantClearances
Dravon Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

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