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

Catheter, Percutaneous, Neurovasculature

21 CFR 870.1250 / Cardiovascular
FDA source (opens on fda.gov)

QJP is the FDA product code for Catheter, Percutaneous, Neurovasculature, a class II device type, regulated under 21 CFR 870.1250. FDA's definition for this code reads: "To provide vascular access to the neurovasculature for interventional or diagnostic procedures". As of , FDA records hold 98 510(k) clearances under this code, the most recent dated , and 7 recalls.

Classification record

Product code
QJP
Device name
Catheter, Percutaneous, Neurovasculature
FDA definition
To provide vascular access to the neurovasculature for interventional or diagnostic procedures
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
100
Ingested recalls
7

Clearances, product code QJP

By decision year
100 clearances under product code QJP with a decision year between 2020 and 2026, 2026 the highest year at 19.
Show the numbers
510(k) clearances under FDA product code QJP by decision year
YearClearances
20209
202112
202214
202314
202418
202514
202619

Applicants with the most clearances

Product code QJP
Applicants holding the most 510(k) clearances under product code QJP
ApplicantClearances
Stryker Corp.9
Route 92 Medical, Head Quarters7
Asahi Intecc Co., Ltd.6
Balt USA, LLC6
Imperative Care Inc.5
Penumbra Inc.5
Perfuze5
Cerenovus, Inc.4
Maduro Medical, Inc.3
Q'apel Medical, Inc.3

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 63 companies shown, in name order