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

Verge™ Microcatheter

K Number: K261610 · Decision Jun 11, 2026
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
174
Applicant Total
10
Review Days
28

Basic Information

Device Name
Verge™ Microcatheter
K Number
K261610
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instylla, Inc.
Date Received
May 14, 2026
Decision Date
June 11, 2026
Product Code
KRA
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
KRA Catheter, Continuous Flush

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