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

Clip, Vena-Cava

21 CFR 870.3260 / Cardiovascular
FDA source (opens on fda.gov)

DST is the FDA product code for Clip, Vena-Cava, a class II device type, regulated under 21 CFR 870.3260. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
DST
Device name
Clip, Vena-Cava
Regulation
21 CFR 870.3260
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
1
Ingested recalls
0

Clearances, product code DST

By decision year
1 clearance under product code DST with a decision year between 1990 and 1990, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code DST by decision year
YearClearances
19901

Applicants with the most clearances

Product code DST
Applicants holding the most 510(k) clearances under product code DST
ApplicantClearances
Medicomp, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code