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

Tembo Embolic System

K Number: K253677 · Decision Dec 15, 2025
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
128
Applicant Total
10
Review Days
24

Basic Information

Device Name
Tembo Embolic System
K Number
K253677
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.3300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Instylla, Inc.
Date Received
November 21, 2025
Decision Date
December 15, 2025
Product Code
KRD
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
KRD Device, Vascular, For Promoting Embolization

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