FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Brite Tip Radianz Guiding Sheath

K Number: K202167 · Decision Feb 26, 2021
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
13
Review Days
207

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Brite Tip Radianz Guiding Sheath
K Number
K202167
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cordis Corporation
Date Received
August 3, 2020
Decision Date
February 26, 2021
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DYB Introducer, Catheter

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DYB), ordered by most recent decision date.

View all

Other Clearances by Cordis Corporation

K Number Device Name
K220654 ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire
K212977 SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands
K210626 SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
K201377 SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter
K201333 SABER .035 PTA Dilatation Catheter
K181592 RAIN Sheath Transradial
K180081 RAILWAY Sheathless Access System
K143412 ADROIT Guiding Catheter
K133843 SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER
K121442 POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
Search all 13 clearances from Cordis Corporation →