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

Saige-Q

K Number: K203517 · Decision Apr 16, 2021
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
39
Applicant Total
10
Review Days
137

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Basic Information

Device Name
Saige-Q
K Number
K203517
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2080
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DeepHealth, Inc.
Date Received
November 30, 2020
Decision Date
April 16, 2021
Product Code
QFM
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
QFM Radiological Computer-Assisted Prioritization Software For Lesions

Similar 510(k) Clearances

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

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Other Clearances by DeepHealth, Inc.

K Number Device Name
K253825 Saige-Dx
K254131 BAC
K251873 Saige-Dx
K243703 TechLive
K243688 Saige-Dx (3.1.0)
K243705 Saige-Density (2.5.0)
K241747 Saige-Dx
K222275 Saige-Density
K220105 Saige-Dx