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

Accessories, A-V Shunt

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

KNZ is the FDA product code for Accessories, A-V Shunt, a class II device type, regulated under 21 CFR 876.5540. As of , FDA records hold 10 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KNZ
Device name
Accessories, A-V Shunt
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
10
Ingested recalls
0

Clearances, product code KNZ

By decision year
10 clearances under product code KNZ with a decision year between 1983 and 1985, 1984 the highest year at 8.
Show the numbers
510(k) clearances under FDA product code KNZ by decision year
YearClearances
19831
19848
19851

Applicants with the most clearances

Product code KNZ
Applicants holding the most 510(k) clearances under product code KNZ
ApplicantClearances
Medical Components, Inc.2
Renal Systems, Inc.2
Argon Medical Corp.1
Intermed, Inc.1
Packaging Technologies, Inc.1
Quinton, Inc.1
Top Surgical Manufacturers Co.1
Vas-Cath of Canada, Ltd.1

Companies listing this code with FDA

Companies whose registered establishments list this code