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

Ziehm Vision RFD

K Number: K203428 · Decision Mar 17, 2021
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
18
Review Days
117

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Basic Information

Device Name
Ziehm Vision RFD
K Number
K203428
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ziehm Imaging GmbH
Date Received
November 20, 2020
Decision Date
March 17, 2021
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

Similar 510(k) Clearances

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Other Clearances by Ziehm Imaging GmbH

K Number Device Name
K243646 Ziehm Solo FD
K243735 Ziehm Vision FD
K243303 Ziehm Vision RFD 3D
K243328 Ziehm Vision RFD
K240099 Ziehm Vision RFD
K240020 Ziehm Vision FD
K234109 Ziehm Solo FD
K231700 Ziehm Vision FD
K231669 Ziehm Solo FD
K231692 Ziehm Vision RFD
Search all 18 clearances from Ziehm Imaging GmbH →