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

Next Generation 088 Catheter

K Number: K254223 · Decision Apr 16, 2026
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
91
Applicant Total
18
Review Days
108

Basic Information

Device Name
Next Generation 088 Catheter
K Number
K254223
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Balt USA, LLC
Date Received
December 29, 2025
Decision Date
April 16, 2026
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

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