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

SIENET CAMERA SERVER

K Number: K923582 · Decision Oct 14, 1992
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
141
Applicant Total
53
Review Days
86

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Basic Information

Device Name
SIENET CAMERA SERVER
K Number
K923582
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.2020
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Gammasonics, Inc.
Date Received
July 20, 1992
Decision Date
October 14, 1992
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

Similar 510(k) Clearances

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Other Clearances by Siemens Gammasonics, Inc.

K Number Device Name
K934766 CARBON FIBER PALLET
K933664 POLYTRON T.O.P. (TIME, OPERATION, PERFORMANCE)
K933256 FAN BEAM COLLIMATOR
K920319 SIENET IMAGE DISPLAY WORKSTATIONS, IMAGE ACQUISITI
K922373 MULTISPECT(TM) 2 DUAL DETECTOR CAMERA SYSTEM
K922372 MULTISPECT(TM) 3 TRIPLE DETECTOR CAMERA SYSTEM
K920310 SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE
K920309 SIENET DIAGNOSTIC REPORTING CONSOLE
K914313 HICOR
K914350 ICON COMPUTER SYSTEM
Search all 53 clearances from Siemens Gammasonics, Inc. →