FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

DigitalDiagnost

K Number: K210692 · Decision Apr 2, 2021
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
18
Review Days
25

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Basic Information

Device Name
DigitalDiagnost
K Number
K210692
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Medical Systems Dmc GmbH
Date Received
March 8, 2021
Decision Date
April 2, 2021
Product Code
KPR
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
KPR System, X-Ray, Stationary

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Other Clearances by Philips Medical Systems Dmc GmbH

K Number Device Name
K233662 Radiography 7300 C
K233678 Radiography 7000 M
K233945 ProxiDiagnost N90 / Precision CRF (706110, 706400)
K232910 CombiDiagnost R90
K212186 Philips Radiology Smart Assistant
K212837 ProxiDiagnost N90
K203087 CombiDiagnost R90
K202564 DigitalDiagnost C90
K182973 DigitalDiagnost C90
K173433 ProxiDiagnost N90
Search all 18 clearances from Philips Medical Systems Dmc GmbH →