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

CARBON FIBER PALLET

K Number: K934766 · Decision Feb 18, 1994
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
53
Review Days
137

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Basic Information

Device Name
CARBON FIBER PALLET
K Number
K934766
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1100
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Gammasonics, Inc.
Date Received
October 4, 1993
Decision Date
February 18, 1994
Product Code
IYX
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
IYX Camera, Scintillation (Gamma)

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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
K914350 ICON COMPUTER SYSTEM
Search all 53 clearances from Siemens Gammasonics, Inc. →