Cleared Traditional

K223189 - Firefighter™ NC Pro PTCA Balloon Catheter (FDA 510(k) Clearance)

Jul 2023
Decision
282d
Days
Class 2
Risk

K223189 is an FDA 510(k) clearance for the Firefighter™ NC Pro PTCA Balloon Catheter. This device is classified as a Catheters, Transluminal Coronary Angioplasty, Percutaneous (Class II - Special Controls, product code LOX).

Submitted by Shanghai MicroPort Medical (Group) Co., Ltd. (Shanghai, CN). The FDA issued a Cleared decision on July 21, 2023, 282 days after receiving the submission on October 12, 2022.

This device falls under the Cardiovascular FDA review panel. Regulated under 21 CFR 870.5100. A Ptca Catheter Is A Device That Operates On The Principle Of Hydraulic Pressurization Applied Through An Inflatable Balloon Attached To The Distal End..

Submission Details

510(k) Number K223189 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 12, 2022
Decision Date July 21, 2023
Days to Decision 282 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary Summary PDF

Device Classification

Product Code LOX - Catheters, Transluminal Coronary Angioplasty, Percutaneous
Device Class Class II - Special Controls
CFR Regulation 21 CFR 870.5100
Definition A Ptca Catheter Is A Device That Operates On The Principle Of Hydraulic Pressurization Applied Through An Inflatable Balloon Attached To The Distal End.