FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

Transpara

K Number: K181704 · Decision Nov 21, 2018
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
34
Applicant Total
7
Review Days
147

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Basic Information

Device Name
Transpara
K Number
K181704
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2090
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Screenpoint Medical B.V.
Date Received
June 27, 2018
Decision Date
November 21, 2018
Product Code
QDQ
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
QDQ Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer

Similar 510(k) Clearances

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

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Other Clearances by Screenpoint Medical B.V.

K Number Device Name
K241831 Transpara (2.1.0)
K232096 Transpara Density 1.0.0
K221347 Transpara 1.7.2
K210404 Transpara 1.7.0
K193229 Transpara
K192287 Transpara