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

Extravascular Support For An Arteriovenous Fistula For Vascular Access

21 CFR 870.4600 / Cardiovascular
FDA source (opens on fda.gov)

QVQ is the FDA product code for Extravascular Support For An Arteriovenous Fistula For Vascular Access, a class II device type, regulated under 21 CFR 870.4600. FDA's definition for this code reads: "This device is a permanent implant which is surgically placed outside and/or around an artery and/or vein to provide external support to arteriovenous fistulas created for vascular access by means of vascular surgery". As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
QVQ
Device name
Extravascular Support For An Arteriovenous Fistula For Vascular Access
FDA definition
This device is a permanent implant which is surgically placed outside and/or around an artery and/or vein to provide external support to arteriovenous fistulas created for vascular access by means of vascular surgery.
Regulation
21 CFR 870.4600
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
2
Ingested recalls
0

Clearances, product code QVQ

By decision year
2 clearances under product code QVQ with a decision year between 2023 and 2024, 2023 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code QVQ by decision year
YearClearances
20231
20241

Applicants with the most clearances

Product code QVQ
Applicants holding the most 510(k) clearances under product code QVQ
ApplicantClearances
Laminate Medical Technologies2

Companies listing this code with FDA

Companies whose registered establishments list this code