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

Amplatzer TorqVue Delivery System

K Number: K260993 · Decision Apr 24, 2026
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
12
Review Days
29

Basic Information

Device Name
Amplatzer TorqVue Delivery System
K Number
K260993
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott
Date Received
March 26, 2026
Decision Date
April 24, 2026
Product Code
DQY
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
DQY Catheter, Percutaneous

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