FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SHIMADZU LATERAL C-ARM MH-30

K Number: K875375 · Decision Feb 12, 1988
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
195
Applicant Total
23
Review Days
43

Basic Information

Device Name
SHIMADZU LATERAL C-ARM MH-30
K Number
K875375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1600
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
SHIMADZU PRECISION INSTRUMENTS, INC.
Date Received
December 31, 1987
Decision Date
February 12, 1988
Product Code
IZI
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
IZI System, X-Ray, Angiographic

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K Number Device Name
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K890913 SDU 800 DIAGNOSTIC ULTRASOUND INSTRUMENT
K884598 SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-1200
K884477 SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150B
K875378 SINGLE PHOTON SET 031 & AZ-701-NTS-SP EMISSION
K882311 SHIMADZU LATERAL C-ARM MH-31
K881674 SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TC
K881795 SHIMADZU X-RAY HIGH VOLTAGE GENERATOR UD150K
K874910 SHIMADZU DIGITAL SUBTRACTION SYSTEM DAR-200
K875370 SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TX
Search all 23 clearances from SHIMADZU PRECISION INSTRUMENTS, INC. →