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

NEURO VISION RADIOGRAPHIC X-RAY SYSTEM

K Number: K904146 · Decision Dec 13, 1990
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
355
Applicant Total
27
Review Days
97

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Basic Information

Device Name
NEURO VISION RADIOGRAPHIC X-RAY SYSTEM
K Number
K904146
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Mallinckrodt Group, Inc.
Date Received
September 7, 1990
Decision Date
December 13, 1990
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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K934664 HYDRAGOWN
K920742 HYDRAJUST IV UROLOGICAL TABLE
K912944 CT 8000 DIGITAL INJECTION SYSTEM
K913264 HYDRAVIEW 1000 DIGITAL IMAGE PROCESS/STOR DEVICE
K905789 FRANKLIN 9000 WALL STAND
K904147 HUGH YOUNG II UROLOGICAL X-RAY SYSTEM
Search all 27 clearances from Mallinckrodt Group, Inc. →