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

Clip, Vascular

21 CFR 870.3250 / Cardiovascular
FDA source (opens on fda.gov)

DSS is the FDA product code for Clip, Vascular, a class II device type, regulated under 21 CFR 870.3250. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
DSS
Device name
Clip, Vascular
Regulation
21 CFR 870.3250
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
8
Ingested recalls
4

Clearances, product code DSS

By decision year
8 clearances under product code DSS with a decision year between 1977 and 1999, 1992 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code DSS by decision year
YearClearances
19771
19881
19901
19923
19961
19991

Applicants with the most clearances

Product code DSS
Applicants holding the most 510(k) clearances under product code DSS
ApplicantClearances
Applied Medical Resources Corp1
Applied Vascular Devices, Inc.1
Axiom Medical, Inc.1
Catheter Research C/O Burditt, Bowles & Radzius1
Heartport, Inc.1
Horizon Surgical, Inc.1
Puritas Health Care, Inc.1
Research Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 14 companies shown, in name order