FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

ArmSure Fluoroscopic Positioning System

K Number: K251992 · Decision Feb 11, 2026
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
1
Review Days
229

Basic Information

Device Name
ArmSure Fluoroscopic Positioning System
K Number
K251992
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Savfe Co. , Ltd.
Date Received
June 27, 2025
Decision Date
February 11, 2026
Product Code
OWB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
OWB Interventional Fluoroscopic X-Ray System

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