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

PowerLook Density Assessment V4.0

K Number: K211506 · Decision Jul 12, 2021
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
303
Applicant Total
14
Review Days
59

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Basic Information

Device Name
PowerLook Density Assessment V4.0
K Number
K211506
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Icad, Inc.
Date Received
May 14, 2021
Decision Date
July 12, 2021
Product Code
QIH
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
QIH Automated Radiological Image Processing Software

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Other Clearances by Icad, Inc.

K Number Device Name
K240417 ProFound Detection (V4.0)
K203822 ProFound AI Software V3.0
K191994 ProFound AI Software V2.1
K182373 PowerLook Tomo Detection V2 Software
K180125 PowerLook Density Assessment Software
K153570 Axxent Electronic Brachytherapy System Model 110 XP 1200
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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