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

PACSNET RESEARCH TOOLKIT

K Number: K905199 · Decision Jan 14, 1991
Classifications
1
FEI Numbers
148
Registration Numbers
148
Same Product Code
141
Applicant Total
53
Review Days
55

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PACSNET RESEARCH TOOLKIT
K Number
K905199
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.2020
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Siemens Gammasonics, Inc.
Date Received
November 20, 1990
Decision Date
January 14, 1991
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

Other 510(k) clearances with the same product code (LMD), ordered by most recent decision date.

View all

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
K923582 SIENET CAMERA SERVER
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
Search all 53 clearances from Siemens Gammasonics, Inc. →