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

Volcano iFR Modality, iFR Scout feature

K Number: K150441 · Decision Mar 20, 2015
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
55
Review Days
28

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Volcano iFR Modality, iFR Scout feature
K Number
K150441
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Volcano Corporation
Date Received
February 20, 2015
Decision Date
March 20, 2015
Product Code
IYO
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IYO), ordered by most recent decision date.

View all

Other Clearances by Volcano Corporation

K Number Device Name
K210235 Verrata PLUS Pressure Guide Wire
K203719 IntraSight Mobile
K202543 OmniWire Pressure Guide Wire, 185 cm Straight Tip, OmniWire Pressure Guide Wire, 185 cm J-Tip
K192886 OmniWire Pressure Guide Wire, 185 cm Straight Tip, OmniWire Pressure Guide Wire, 185 cm J-Tip
K190626 SyncVision System
K190078 IntraSight
K173860 s5 Intravascular Ultrasound Imaging and Pressure Systems, s5i Intravascular Ultrasound Imaging and Pressure Systems, CORE Precision Guided Therapy System, CORE Mobile Precision Guided Therapy System
K172455 CORE M2 Vascular System, CORE M2 Software v4.2 Upgrade Kit, CORE M2 Software v4.2 Installation Kit
K172574 SyncVision System
K170385 CORE M2 Vascular System
Search all 55 clearances from Volcano Corporation →