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

Axxent Electronic Brachytherapy System Model 110 XP 1200

K Number: K153570 · Decision Feb 25, 2016
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
52
Applicant Total
14
Review Days
73

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Basic Information

Device Name
Axxent Electronic Brachytherapy System Model 110 XP 1200
K Number
K153570
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5900
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Icad, Inc.
Date Received
December 14, 2015
Decision Date
February 25, 2016
Product Code
JAD
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
JAD System, Therapeutic, X-Ray

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Other Clearances by Icad, Inc.

K Number Device Name
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K203822 ProFound AI Software V3.0
K191994 ProFound AI Software V2.1
K182373 PowerLook Tomo Detection V2 Software
K180125 PowerLook Density Assessment Software
K141343 AXXENT CERVICAL APPLICATOR
K123442 XOFT AXXENT CERVICAL APPLICATORS
K122951 XOFT AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM MODEL 110
K121517 VERSAVUE ENTERPRISE SUITE
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