Product code DRE— Cardiovascular

VESSEL DILATOR

Classification name: Dilator, Vessel, For Percutaneous Catheterization
Device class: Class 2
Regulation: 21 CFR 870.1310
Advisory panel: Cardiovascular
Total cleared: 105
First cleared: 1976-08-23
Most recent: 2026-07-27

Clearances under product code DRE — page 2

101–105 of 105

K802327 — SHEATH DILATOR SETStanco Medical, Inc.·1980-10-10
K801113 — DILATOR, VESSEL, FOR PERC. CATHETER.Alva Medical, Inc.·1980-07-28
K800462 — PERCUTANEOUS INTRODUCER SETMedical Components, Inc.·1980-03-19
K780126 — DILATOR, VESSEL & INTRODUCER, SHEATHArgon Medical Corp.·1978-03-02
K760403 — TEMPORARY ATRIAL ELECTRODE KITUsci, Div. C.R. Bard, Inc.·1976-08-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.