510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
DWQClass II

Stripper, Vein, External

21 CFR 870.4885 / Cardiovascular
FDA source (opens on fda.gov)

DWQ is the FDA product code for Stripper, Vein, External, a class II device type, regulated under 21 CFR 870.4885. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and 2 recalls.

Classification record

Product code
DWQ
Device name
Stripper, Vein, External
Regulation
21 CFR 870.4885
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
8
Ingested recalls
2

Clearances, product code DWQ

By decision year
8 clearances under product code DWQ with a decision year between 1981 and 2022, 1991 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code DWQ by decision year
YearClearances
19811
19871
19901
19912
20031
20041
20221

Applicants with the most clearances

Product code DWQ
Applicants holding the most 510(k) clearances under product code DWQ
ApplicantClearances
Smith & Nephew, Inc.2
Aesculap Instruments Corp.1
Atrium Medical Corporation1
LeMaitre Vascular Inc.1
Pilling Co.1
Solco Basle, Inc.1
Uresil, LLC1

Companies listing this code with FDA

Companies whose registered establishments list this code