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

Occluder, Catheter Tip

21 CFR 870.1370 / Cardiovascular
FDA source (opens on fda.gov)

DQT is the FDA product code for Occluder, Catheter Tip, a class II device type, regulated under 21 CFR 870.1370. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
DQT
Device name
Occluder, Catheter Tip
Regulation
21 CFR 870.1370
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
Yes
Ingested clearances
12
Ingested recalls
4

Clearances, product code DQT

By decision year
12 clearances under product code DQT with a decision year between 1984 and 1999, 1987 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code DQT by decision year
YearClearances
19841
19851
19861
19873
19882
19912
19951
19991

Applicants with the most clearances

Product code DQT
Applicants holding the most 510(k) clearances under product code DQT
ApplicantClearances
Ideas for Medicine, Inc.3
Advanced Cardiovascular Systems, Inc.1
Applied Vascular Devices, Inc.1
Arterial Vascular Engineering, Inc.1
BD Becton Dickinson Vacutainer Systems Preanalytic1
Cathlab Corp.1
Clincal Instruments Corp.1
Dlp, Inc.1
Micro Interventional Systems, Inc.1
Uresil, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code