FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SIENET DICOM GATEWAY

K Number: K952533 · Decision Aug 23, 1995
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
141
Applicant Total
15
Review Days
83

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Basic Information

Device Name
SIENET DICOM GATEWAY
K Number
K952533
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.2020
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens AG
Date Received
June 1, 1995
Decision Date
August 23, 1995
Product Code
LMD
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
LMD System, Digital Image Communications, Radiological

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K043122 SMD 21500 OR DSB-2103-D-5MP-5M PIXEL GRAYSCALE FLAT PANEL DISPLAY
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