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

ECT CARBON FIBER PALLET, MODIFICATION

K Number: K912481 · Decision Aug 2, 1991
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
11
Applicant Total
53
Review Days
71

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Basic Information

Device Name
ECT CARBON FIBER PALLET, MODIFICATION
K Number
K912481
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1350
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Siemens Gammasonics, Inc.
Date Received
May 23, 1991
Decision Date
August 2, 1991
Product Code
IYZ
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
IYZ Bed, Scanning, Nuclear

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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
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. →