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

Carrier XL Delivery Catheter

K Number: K252569 · Decision Oct 22, 2025
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
91
Applicant Total
18
Review Days
69

Basic Information

Device Name
Carrier XL Delivery Catheter
K Number
K252569
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Balt USA, LLC
Date Received
August 14, 2025
Decision Date
October 22, 2025
Product Code
QJP
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
QJP Catheter, Percutaneous, Neurovasculature

Similar 510(k) Clearances

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

View all

Other Clearances by Balt USA, LLC

K Number Device Name
K254223 Next Generation 088 Catheter
K254221 Optima Coil System (OptiOne Coil System)
K252700 Optima Coil System (Optima Packing Coil System)
K243948 Raptor Aspiration Catheter; Balt Aspiration Tubing Set
K251383 Prestige Coil System (Prestige Packing Line Extension)
K242376 Next Generation Access Platform
K242582 Optima Coil System (OptiBlock Line Extension)
K234074 Next Generation Access Catheter
K234083 Next Generation Aspiration Catheter; Balt Aspiration Tubing Set
K230609 NG Delivery Catheter
Search all 18 clearances from Balt USA, LLC →