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

Identify (4.0)

K Number: K242957 · Decision Feb 7, 2025
Classifications
1
FEI Numbers
123
Registration Numbers
124
Same Product Code
717
Applicant Total
49
Review Days
135

Basic Information

Device Name
Identify (4.0)
K Number
K242957
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Varian Medical Systems, Inc.
Date Received
September 25, 2024
Decision Date
February 7, 2025
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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Other Clearances by Varian Medical Systems, Inc.

K Number Device Name
K250299 CT/ MR Tandem and Ovoid Set
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K242608 Embozene Color-Advanced Microspheres
K241764 Mould Probe MR Safe
K242874 Gating Reflector Block
K241853 Titanium Fletcher-Style Applicator Set Defined Geometry; Smit Cervical Sleeve
K242794 ONCOZENE Microspheres
K241386 Heyman Packing Applicator Set (GM11004580)
K240480 IntelliBlate Microwave Ablation System Console (IB-CON); IntelliBlate Microwave Ablation System Mobile Cart (IB-CART); IntelliBlate Ximitry Probe Assembly, 13G x 15cm (IB-XPA-1315); IntelliBlate Ximitry Probe Assembly, 13G x 20cm (IB-XPA-1320); IntelliBlate Ximitry Probe Assembly, 13G x 27cm (IB-XPA-1327)
K240784 Temperature Sensor Probe (ABL-18TP20)
Search all 49 clearances from Varian Medical Systems, Inc. →